Canonical Allele Identifier: CA8600642
Community Standard Title: NM_000342.4(SLC4A1):c.331C>T (p.Arg111Cys)
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44260653G>A , CM000679.2:g.44260653G>A GRCh38
NC_000017.10:g.42338021G>A , CM000679.1:g.42338021G>A GRCh37
NC_000017.9:g.39693547G>A NCBI36
NG_007498.1:g.12482C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000342.4:c.331C>T MANE Select NP_000333.1:p.Arg111Cys
ENST00000262418.12:c.331C>T MANE Select ENSP00000262418.6:p.Arg111Cys
NM_000342.3:c.331C>T NP_000333.1:p.Arg111Cys
ENST00000262418.10:c.331C>T ENSP00000262418.6:p.Arg111Cys
ENST00000399246.3:c.331C>T ENSP00000382190.3:p.Arg111Cys
ENST00000471005.5:n.265C>T
ENST00000497360.5:n.470C>T
XM_005257593.3:c.136C>T XP_005257650.1:p.Arg46Cys
XM_005257593.5:c.136C>T XP_005257650.1:p.Arg46Cys
XM_011525129.1:c.331C>T XP_011523431.1:p.Arg111Cys
XM_011525129.2:c.331C>T XP_011523431.1:p.Arg111Cys
XM_011525130.1:c.331C>T XP_011523432.1:p.Arg111Cys
XM_011525131.1:c.331C>T XP_011523433.1:p.Arg111Cys