Canonical Allele Identifier: CA7654399

Gene: STRA6

Linked Data

• dbSNP Id: rs146105072
• ExAC: 15:74472535 G / A
• gnomAD v2: 15-74472535-G-A
• gnomAD v3: 15-74180194-G-A
• gnomAD v4: 15-74180194-G-A
• MyVariant Identifiers: chr15:g.74472535G>A (hg19) ; chr15:g.74180194G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74180194G>A , CM000677.2:g.74180194G>A	GRCh38
NC_000015.9:g.74472535G>A , CM000677.1:g.74472535G>A	GRCh37
NC_000015.8:g.72259588G>A	NCBI36
NG_009207.1:g.33837C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395105.9:c.1890C>T MANE Select	ENSP00000378537.4:p.Pro630=
ENST00000323940.9:c.1890C>T	ENSP00000326085.5:p.Pro630=
ENST00000395105.8:c.1890C>T	ENSP00000378537.4:p.Pro630=
ENST00000416286.7:c.1866C>T	ENSP00000400403.3:p.Pro622=
ENST00000423167.6:c.1863C>T	ENSP00000413012.2:p.Pro621=
ENST00000449139.6:c.1890C>T	ENSP00000410221.2:p.Pro630=
ENST00000535552.5:c.2001C>T	ENSP00000440238.1:p.Pro667=
ENST00000545137.5:n.1599C>T
ENST00000563965.5:c.2007C>T	ENSP00000456609.1:p.Pro669=
ENST00000572785.1:c.745C>T
ENST00000574278.5:c.1935C>T	ENSP00000458827.1:p.Pro645=
ENST00000574439.5:n.2162C>T
ENST00000616000.4:c.1890C>T	ENSP00000479112.1:p.Pro630=
NM_001142617.1:c.1890C>T	NP_001136089.1:p.Pro630=
NM_001142618.1:c.1890C>T	NP_001136090.1:p.Pro630=
NM_001142619.1:c.1863C>T	NP_001136091.1:p.Pro621=
NM_001199040.1:c.2001C>T	NP_001185969.1:p.Pro667=
NM_001199041.1:c.1935C>T	NP_001185970.1:p.Pro645=
NM_001199042.1:c.2007C>T	NP_001185971.1:p.Pro669=
NM_022369.3:c.1890C>T	NP_071764.3:p.Pro630=
XM_011521883.1:c.1890C>T	XP_011520185.1:p.Pro630=
XM_011521884.1:c.1701C>T	XP_011520186.1:p.Pro567=
XM_017022478.1:c.1938C>T	XP_016877967.1:p.Pro646=
XM_017022479.1:c.1890C>T	XP_016877968.1:p.Pro630=
XM_017022480.1:c.1701C>T	XP_016877969.1:p.Pro567=
NM_022369.4:c.1890C>T MANE Select	NP_071764.3:p.Pro630=
NM_001142617.2:c.1890C>T	NP_001136089.1:p.Pro630=
NM_001142619.2:c.1863C>T	NP_001136091.1:p.Pro621=
NM_001199042.2:c.2007C>T	NP_001185971.1:p.Pro669=
NM_001142618.2:c.1890C>T	NP_001136090.1:p.Pro630=
NM_001199040.2:c.2001C>T	NP_001185969.1:p.Pro667=
NM_001199041.2:c.1935C>T	NP_001185970.1:p.Pro645=