Canonical Allele Identifier: CA351050578

Gene: SAG

Linked Data

• MyVariant Identifiers: chr2:g.234255543T>A (hg19) ; chr2:g.233346897T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346897T>A , CM000664.2:g.233346897T>A	GRCh38
NC_000002.11:g.234255543T>A , CM000664.1:g.234255543T>A	GRCh37
NC_000002.10:g.233920282T>A	NCBI36
NG_009116.1:g.44235T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1203T>A MANE Select	ENSP00000386444.1:p.Asn401Lys
ENST00000409110.5:c.1203T>A	ENSP00000386444.1:p.Asn401Lys
ENST00000412969.6:n.2423T>A
ENST00000471884.5:n.3234T>A
ENST00000474220.5:n.409T>A
ENST00000476500.5:n.6502T>A
ENST00000492629.1:n.164T>A
NM_000541.4:c.1203T>A	NP_000532.2:p.Asn401Lys
XM_011511589.1:c.1203T>A	XP_011509891.1:p.Asn401Lys
XM_011511590.1:c.1203T>A	XP_011509892.1:p.Asn401Lys
XM_011511591.1:c.*71T>A	XP_011509893.1:n.*71T>A
XM_011511592.1:c.1047T>A	XP_011509894.1:p.Asn349Lys
XM_011511593.1:c.903T>A	XP_011509895.1:p.Asn301Lys
XM_011511594.1:c.831T>A	XP_011509896.1:p.Asn277Lys
XM_011511596.1:c.801T>A	XP_011509898.1:p.Asn267Lys
XM_011511597.1:c.801T>A	XP_011509899.1:p.Asn267Lys
XR_922978.1:n.1520T>A
XR_922980.1:n.1619T>A
XM_011511593.3:c.903T>A	XP_011509895.1:p.Asn301Lys
XM_017004641.1:c.*71T>A	XP_016860130.1:n.*71T>A
XM_024453036.1:c.*71T>A	XP_024308804.1:n.*71T>A
XR_001738882.1:n.1401T>A
XR_922980.2:n.1619T>A
NM_000541.5:c.1203T>A MANE Select	NP_000532.2:p.Asn401Lys