Canonical Allele Identifier: CA384320849

Gene: SOX5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.23740992T>C , CM000674.2:g.23740992T>C	GRCh38
NC_000012.11:g.23893926T>C , CM000674.1:g.23893926T>C	GRCh37
NC_000012.10:g.23785193T>C	NCBI36
NG_029612.1:g.826455A>G
NG_029612.2:g.826455A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704298.1:c.577A>G	ENSP00000515822.1:p.Ile193Val
ENST00000704299.1:c.472A>G	ENSP00000515823.1:p.Ile158Val
ENST00000704300.1:c.577A>G	ENSP00000515824.1:p.Ile193Val
ENST00000451604.7:c.616A>G MANE Select	ENSP00000398273.2:p.Ile206Val
ENST00000646273.1:c.577A>G	ENSP00000493866.1:p.Ile193Val
ENST00000659413.1:c.472A>G	ENSP00000499309.1:p.Ile158Val
ENST00000367206.7:c.586A>G	ENSP00000356174.3:p.Ile196Val
ENST00000381381.6:c.577A>G	ENSP00000370788.2:p.Ile193Val
ENST00000451604.6:c.616A>G	ENSP00000398273.2:p.Ile206Val
ENST00000537393.5:c.511A>G	ENSP00000439832.1:p.Ile171Val
ENST00000541536.5:c.577A>G	ENSP00000441973.1:p.Ile193Val
ENST00000541847.5:c.586A>G	ENSP00000442119.1:p.Ile196Val
ENST00000545921.5:c.586A>G	ENSP00000443520.1:p.Ile196Val
ENST00000546136.5:c.577A>G	ENSP00000437487.1:p.Ile193Val
NM_001261414.1:c.577A>G	NP_001248343.1:p.Ile193Val
NM_001261415.1:c.586A>G	NP_001248344.1:p.Ile196Val
NM_006940.4:c.616A>G	NP_008871.3:p.Ile206Val
NM_152989.3:c.577A>G	NP_694534.1:p.Ile193Val
XM_006719149.2:c.577A>G	XP_006719212.1:p.Ile193Val
XM_011520831.1:c.511A>G	XP_011519133.1:p.Ile171Val
XM_011520832.1:c.616A>G	XP_011519134.1:p.Ile206Val
XM_011520833.1:c.586A>G	XP_011519135.1:p.Ile196Val
XM_011520834.1:c.577A>G	XP_011519136.1:p.Ile193Val
XM_011520835.1:c.577A>G	XP_011519137.1:p.Ile193Val
XM_011520836.1:c.577A>G	XP_011519138.1:p.Ile193Val
XM_011520837.1:c.577A>G	XP_011519139.1:p.Ile193Val
XM_011520838.1:c.511A>G	XP_011519140.1:p.Ile171Val
XM_011520839.1:c.472A>G	XP_011519141.1:p.Ile158Val
XR_931436.1:n.207+2136T>C
NM_001261414.2:c.577A>G	NP_001248343.1:p.Ile193Val
NM_001261415.2:c.586A>G	NP_001248344.1:p.Ile196Val
NM_001330785.1:c.511A>G	NP_001317714.1:p.Ile171Val
NM_006940.5:c.616A>G	NP_008871.3:p.Ile206Val
NM_152989.4:c.577A>G	NP_694534.1:p.Ile193Val
XM_011520832.2:c.616A>G	XP_011519134.1:p.Ile206Val
XM_011520833.2:c.586A>G	XP_011519135.1:p.Ile196Val
XM_011520834.2:c.577A>G	XP_011519136.1:p.Ile193Val
XM_011520835.2:c.577A>G	XP_011519137.1:p.Ile193Val
XM_011520837.2:c.577A>G	XP_011519139.1:p.Ile193Val
XM_011520838.2:c.511A>G	XP_011519140.1:p.Ile171Val
XM_017019888.1:c.703A>G	XP_016875377.1:p.Ile235Val
XM_017019889.1:c.703A>G	XP_016875378.1:p.Ile235Val
XM_017019890.1:c.577A>G	XP_016875379.1:p.Ile193Val
XM_017019891.1:c.577A>G	XP_016875380.1:p.Ile193Val
XM_017019892.1:c.577A>G	XP_016875381.1:p.Ile193Val
XM_017019893.1:c.577A>G	XP_016875382.1:p.Ile193Val
XM_017019894.1:c.577A>G	XP_016875383.1:p.Ile193Val
XM_017019895.1:c.577A>G	XP_016875384.1:p.Ile193Val
XM_017019896.1:c.577A>G	XP_016875385.1:p.Ile193Val
XM_017019897.1:c.472A>G	XP_016875386.1:p.Ile158Val
XM_017019898.1:c.472A>G	XP_016875387.1:p.Ile158Val
XM_017019899.1:c.472A>G	XP_016875388.1:p.Ile158Val
XM_017019900.1:c.472A>G	XP_016875389.1:p.Ile158Val
XM_017019901.1:c.472A>G	XP_016875390.1:p.Ile158Val
XM_017019902.1:c.616A>G	XP_016875391.1:p.Ile206Val
XM_017019903.1:c.616A>G	XP_016875392.1:p.Ile206Val
XM_024449150.1:c.577A>G	XP_024304918.1:p.Ile193Val
XM_024449151.1:c.577A>G	XP_024304919.1:p.Ile193Val
XM_024449152.1:c.577A>G	XP_024304920.1:p.Ile193Val
XM_024449153.1:c.577A>G	XP_024304921.1:p.Ile193Val
XM_024449154.1:c.577A>G	XP_024304922.1:p.Ile193Val
XM_024449155.1:c.577A>G	XP_024304923.1:p.Ile193Val
XM_024449157.1:c.577A>G	XP_024304925.1:p.Ile193Val
XM_024449158.1:c.577A>G	XP_024304926.1:p.Ile193Val
XM_024449159.1:c.577A>G	XP_024304927.1:p.Ile193Val
XM_024449160.1:c.577A>G	XP_024304928.1:p.Ile193Val
XM_024449161.1:c.577A>G	XP_024304929.1:p.Ile193Val
XM_024449163.1:c.472A>G	XP_024304931.1:p.Ile158Val
XM_024449164.1:c.472A>G	XP_024304932.1:p.Ile158Val
XM_024449165.1:c.472A>G	XP_024304933.1:p.Ile158Val
NM_006940.6:c.616A>G MANE Select	NP_008871.3:p.Ile206Val
NM_001261414.3:c.577A>G	NP_001248343.1:p.Ile193Val
NM_001330785.2:c.511A>G	NP_001317714.1:p.Ile171Val
NM_152989.5:c.577A>G	NP_694534.1:p.Ile193Val
NM_001261415.3:c.586A>G	NP_001248344.1:p.Ile196Val