Canonical Allele Identifier: CA351050281
Gene: SAG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233346825A>T , CM000664.2:g.233346825A>T GRCh38
NC_000002.11:g.234255471A>T , CM000664.1:g.234255471A>T GRCh37
NC_000002.10:g.233920210A>T NCBI36
NG_009116.1:g.44163A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409110.6:c.1131A>T MANE Select ENSP00000386444.1:p.Leu377Phe
ENST00000409110.5:c.1131A>T ENSP00000386444.1:p.Leu377Phe
ENST00000412969.6:n.2351A>T
ENST00000471884.5:n.3162A>T
ENST00000474220.5:n.337A>T
ENST00000476500.5:n.6430A>T
ENST00000492629.1:n.92A>T
NM_000541.4:c.1131A>T NP_000532.2:p.Leu377Phe
XM_011511589.1:c.1131A>T XP_011509891.1:p.Leu377Phe
XM_011511590.1:c.1131A>T XP_011509892.1:p.Leu377Phe
XM_011511591.1:c.1121A>T XP_011509893.1:p.Ter374Leu
XM_011511592.1:c.975A>T XP_011509894.1:p.Leu325Phe
XM_011511593.1:c.831A>T XP_011509895.1:p.Leu277Phe
XM_011511594.1:c.759A>T XP_011509896.1:p.Leu253Phe
XM_011511596.1:c.729A>T XP_011509898.1:p.Leu243Phe
XM_011511597.1:c.729A>T XP_011509899.1:p.Leu243Phe
XR_922978.1:n.1448A>T
XR_922979.1:n.1452A>T
XR_922980.1:n.1547A>T
XM_011511593.3:c.831A>T XP_011509895.1:p.Leu277Phe
XM_017004641.1:c.1121A>T XP_016860130.1:p.Ter374Leu
XM_024453036.1:c.719A>T XP_024308804.1:p.Ter240Leu
XR_001738882.1:n.1329A>T
XR_922980.2:n.1547A>T
NM_000541.5:c.1131A>T MANE Select NP_000532.2:p.Leu377Phe