Canonical Allele Identifier: CA351050312

Gene: SAG

Linked Data

• dbSNP Id: rs1701267610
• MyVariant Identifiers: chr2:g.234255484T>C (hg19) ; chr2:g.233346838T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346838T>C , CM000664.2:g.233346838T>C	GRCh38
NC_000002.11:g.234255484T>C , CM000664.1:g.234255484T>C	GRCh37
NC_000002.10:g.233920223T>C	NCBI36
NG_009116.1:g.44176T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1144T>C MANE Select	ENSP00000386444.1:p.Phe382Leu
ENST00000409110.5:c.1144T>C	ENSP00000386444.1:p.Phe382Leu
ENST00000412969.6:n.2364T>C
ENST00000471884.5:n.3175T>C
ENST00000474220.5:n.350T>C
ENST00000476500.5:n.6443T>C
ENST00000492629.1:n.105T>C
NM_000541.4:c.1144T>C	NP_000532.2:p.Phe382Leu
XM_011511589.1:c.1144T>C	XP_011509891.1:p.Phe382Leu
XM_011511590.1:c.1144T>C	XP_011509892.1:p.Phe382Leu
XM_011511591.1:c.*12T>C	XP_011509893.1:n.*12T>C
XM_011511592.1:c.988T>C	XP_011509894.1:p.Phe330Leu
XM_011511593.1:c.844T>C	XP_011509895.1:p.Phe282Leu
XM_011511594.1:c.772T>C	XP_011509896.1:p.Phe258Leu
XM_011511596.1:c.742T>C	XP_011509898.1:p.Phe248Leu
XM_011511597.1:c.742T>C	XP_011509899.1:p.Phe248Leu
XR_922978.1:n.1461T>C
XR_922979.1:n.1465T>C
XR_922980.1:n.1560T>C
XM_011511593.3:c.844T>C	XP_011509895.1:p.Phe282Leu
XM_017004641.1:c.*12T>C	XP_016860130.1:n.*12T>C
XM_024453036.1:c.*12T>C	XP_024308804.1:n.*12T>C
XR_001738882.1:n.1342T>C
XR_922980.2:n.1560T>C
NM_000541.5:c.1144T>C MANE Select	NP_000532.2:p.Phe382Leu