Canonical Allele Identifier: CA2174362

Gene: SAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233322990A>G , CM000664.2:g.233322990A>G	GRCh38
NC_000002.11:g.234231636A>G , CM000664.1:g.234231636A>G	GRCh37
NC_000002.10:g.233896375A>G	NCBI36
NG_009116.1:g.20328A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000541.5:c.420A>G MANE Select	NP_000532.2:p.Pro140=
ENST00000409110.6:c.420A>G MANE Select	ENSP00000386444.1:p.Pro140=
NM_000541.4:c.420A>G	NP_000532.2:p.Pro140=
ENST00000409110.5:c.420A>G	ENSP00000386444.1:p.Pro140=
ENST00000412969.6:n.360A>G
ENST00000447536.5:c.420A>G	ENSP00000408937.1:p.Pro140=
ENST00000453143.5:c.*251A>G	ENSP00000404733.1:n.*251A>G
ENST00000471884.5:n.591A>G
ENST00000474206.1:n.257A>G
ENST00000476500.5:n.461A>G
ENST00000479450.1:n.184A>G
XM_011511589.1:c.420A>G	XP_011509891.1:p.Pro140=
XM_011511590.1:c.420A>G	XP_011509892.1:p.Pro140=
XM_011511591.1:c.420A>G	XP_011509893.1:p.Pro140=
XM_011511592.1:c.264A>G	XP_011509894.1:p.Pro88=
XM_011511593.1:c.120A>G	XP_011509895.1:p.Pro40=
XM_011511593.3:c.120A>G	XP_011509895.1:p.Pro40=
XM_011511594.1:c.48A>G	XP_011509896.1:p.Pro16=
XM_011511595.1:c.420A>G	XP_011509897.1:p.Pro140=
XM_011511596.1:c.18A>G	XP_011509898.1:p.Pro6=
XM_011511597.1:c.18A>G	XP_011509899.1:p.Pro6=
XM_017004641.1:c.420A>G	XP_016860130.1:p.Pro140=
XM_017004642.1:c.420A>G	XP_016860131.1:p.Pro140=
XM_017004643.1:c.420A>G	XP_016860132.1:p.Pro140=
XM_024453036.1:c.18A>G	XP_024308804.1:p.Pro6=
XR_001738882.1:n.497A>G
XR_922978.1:n.616A>G
XR_922979.1:n.616A>G
XR_922980.1:n.715A>G
XR_922980.2:n.715A>G