Canonical Allele Identifier: CA1640421
Community Standard Title: NM_000341.4(SLC3A1):c.1126G>A (p.Gly376Ser)
Gene: SLC3A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44301117G>A , CM000664.2:g.44301117G>A GRCh38
NC_000002.11:g.44528256G>A , CM000664.1:g.44528256G>A GRCh37
NC_000002.10:g.44381760G>A NCBI36
NG_008233.1:g.30660G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000341.4:c.1126G>A MANE Select NP_000332.2:p.Gly376Ser
ENST00000260649.11:c.1126G>A MANE Select ENSP00000260649.6:p.Gly376Ser
NM_000341.3:c.1126G>A NP_000332.2:p.Gly376Ser
ENST00000260649.10:c.1126G>A ENSP00000260649.6:p.Gly376Ser
ENST00000409229.7:c.1126G>A ENSP00000386620.3:p.Gly376Ser
ENST00000409294.5:c.-5+1027G>A ENSP00000386852.1:n.-5+1027G>A
ENST00000409380.5:c.292G>A ENSP00000386709.1:p.Gly98Ser
ENST00000409387.5:c.1126G>A ENSP00000387308.1:p.Gly376Ser
ENST00000409741.5:c.1126G>A ENSP00000386954.1:p.Gly376Ser
ENST00000410056.7:c.1126G>A ENSP00000387337.3:p.Gly376Ser
ENST00000611973.4:c.1126G>A ENSP00000483618.1:p.Gly376Ser
ENST00000649044.1:c.*1137G>A ENSP00000497083.1:n.*1137G>A
XM_011533047.1:c.1126G>A XP_011531349.1:p.Gly376Ser
XM_011533047.3:c.1126G>A XP_011531349.1:p.Gly376Ser