Canonical Allele Identifier: CA351050484

Gene: SAG

Linked Data

• MyVariant Identifiers: chr2:g.234255524A>T (hg19) ; chr2:g.233346878A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346878A>T , CM000664.2:g.233346878A>T	GRCh38
NC_000002.11:g.234255524A>T , CM000664.1:g.234255524A>T	GRCh37
NC_000002.10:g.233920263A>T	NCBI36
NG_009116.1:g.44216A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1184A>T MANE Select	ENSP00000386444.1:p.Glu395Val
ENST00000409110.5:c.1184A>T	ENSP00000386444.1:p.Glu395Val
ENST00000412969.6:n.2404A>T
ENST00000471884.5:n.3215A>T
ENST00000474220.5:n.390A>T
ENST00000476500.5:n.6483A>T
ENST00000492629.1:n.145A>T
NM_000541.4:c.1184A>T	NP_000532.2:p.Glu395Val
XM_011511589.1:c.1184A>T	XP_011509891.1:p.Glu395Val
XM_011511590.1:c.1184A>T	XP_011509892.1:p.Glu395Val
XM_011511591.1:c.*52A>T	XP_011509893.1:n.*52A>T
XM_011511592.1:c.1028A>T	XP_011509894.1:p.Glu343Val
XM_011511593.1:c.884A>T	XP_011509895.1:p.Glu295Val
XM_011511594.1:c.812A>T	XP_011509896.1:p.Glu271Val
XM_011511596.1:c.782A>T	XP_011509898.1:p.Glu261Val
XM_011511597.1:c.782A>T	XP_011509899.1:p.Glu261Val
XR_922978.1:n.1501A>T
XR_922980.1:n.1600A>T
XM_011511593.3:c.884A>T	XP_011509895.1:p.Glu295Val
XM_017004641.1:c.*52A>T	XP_016860130.1:n.*52A>T
XM_024453036.1:c.*52A>T	XP_024308804.1:n.*52A>T
XR_001738882.1:n.1382A>T
XR_922980.2:n.1600A>T
NM_000541.5:c.1184A>T MANE Select	NP_000532.2:p.Glu395Val