Canonical Allele Identifier: CA2663686034

Gene: SAG

Linked Data

• gnomAD v4: 2-233346919-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346919C>A , CM000664.2:g.233346919C>A	GRCh38
NC_000002.11:g.234255565C>A , CM000664.1:g.234255565C>A	GRCh37
NC_000002.10:g.233920304C>A	NCBI36
NG_009116.1:g.44257C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000409110.6:c.*7C>A MANE Select	ENSP00000386444.1:n.*7C>A
ENST00000409110.5:c.*7C>A	ENSP00000386444.1:n.*7C>A
ENST00000412969.6:n.2445C>A
ENST00000471884.5:n.3256C>A
ENST00000474220.5:n.431C>A
ENST00000476500.5:n.6524C>A
ENST00000492629.1:n.186C>A
NM_000541.4:c.*7C>A	NP_000532.2:n.*7C>A
XM_011511589.1:c.*7C>A	XP_011509891.1:n.*7C>A
XM_011511590.1:c.*7C>A	XP_011509892.1:n.*7C>A
XM_011511591.1:c.*93C>A	XP_011509893.1:n.*93C>A
XM_011511592.1:c.*7C>A	XP_011509894.1:n.*7C>A
XM_011511593.1:c.*7C>A	XP_011509895.1:n.*7C>A
XM_011511594.1:c.*7C>A	XP_011509896.1:n.*7C>A
XM_011511596.1:c.*7C>A	XP_011509898.1:n.*7C>A
XM_011511597.1:c.*7C>A	XP_011509899.1:n.*7C>A
XR_922978.1:n.1542C>A
XR_922980.1:n.1641C>A
XM_011511593.3:c.*7C>A	XP_011509895.1:n.*7C>A
XM_017004641.1:c.*93C>A	XP_016860130.1:n.*93C>A
XM_024453036.1:c.*93C>A	XP_024308804.1:n.*93C>A
XR_001738882.1:n.1423C>A
XR_922980.2:n.1641C>A
NM_000541.5:c.*7C>A MANE Select	NP_000532.2:n.*7C>A