Canonical Allele Identifier: CA2261307651
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44253150C= , CM000679.2:g.44253150C= GRCh38
NC_000017.10:g.42330518C= , CM000679.1:g.42330518C= GRCh37
NC_000017.9:g.39686044C= NCBI36
NG_007498.1:g.19985G=

Transcript Alleles

HGVS Amino-acid Change
NM_000342.4:c.2279G= MANE Select NP_000333.1:p.Arg760=
ENST00000262418.12:c.2279G= MANE Select ENSP00000262418.6:p.Arg760=
NM_000342.3:c.2279G= NP_000333.1:p.Arg760=
ENST00000262418.10:c.2279G= ENSP00000262418.6:p.Arg760=
ENST00000399246.3:c.1181G= ENSP00000382190.3:p.Arg394=
XM_005257593.3:c.2084G= XP_005257650.1:p.Arg695=
XM_005257593.5:c.2084G= XP_005257650.1:p.Arg695=
XM_011525129.1:c.2189G= XP_011523431.1:p.Arg730=
XM_011525129.2:c.2189G= XP_011523431.1:p.Arg730=
XM_011525130.1:c.2279G= XP_011523432.1:p.Arg760=