Canonical Allele Identifier: CA1640420
Community Standard Title: NM_000341.4(SLC3A1):c.1125C>T (p.Pro375=)
Gene: SLC3A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44301116C>T , CM000664.2:g.44301116C>T GRCh38
NC_000002.11:g.44528255C>T , CM000664.1:g.44528255C>T GRCh37
NC_000002.10:g.44381759C>T NCBI36
NG_008233.1:g.30659C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000341.4:c.1125C>T MANE Select NP_000332.2:p.Pro375=
ENST00000260649.11:c.1125C>T MANE Select ENSP00000260649.6:p.Pro375=
NM_000341.3:c.1125C>T NP_000332.2:p.Pro375=
ENST00000260649.10:c.1125C>T ENSP00000260649.6:p.Pro375=
ENST00000409229.7:c.1125C>T ENSP00000386620.3:p.Pro375=
ENST00000409294.5:c.-5+1026C>T ENSP00000386852.1:n.-5+1026C>T
ENST00000409380.5:c.291C>T ENSP00000386709.1:p.Pro97=
ENST00000409387.5:c.1125C>T ENSP00000387308.1:p.Pro375=
ENST00000409741.5:c.1125C>T ENSP00000386954.1:p.Pro375=
ENST00000410056.7:c.1125C>T ENSP00000387337.3:p.Pro375=
ENST00000611973.4:c.1125C>T ENSP00000483618.1:p.Pro375=
ENST00000649044.1:c.*1136C>T ENSP00000497083.1:n.*1136C>T
XM_011533047.1:c.1125C>T XP_011531349.1:p.Pro375=
XM_011533047.3:c.1125C>T XP_011531349.1:p.Pro375=