Canonical Allele Identifier: CA2261307710
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44253327C= , CM000679.2:g.44253327C= GRCh38
NC_000017.10:g.42330695C= , CM000679.1:g.42330695C= GRCh37
NC_000017.9:g.39686221C= NCBI36
NG_007498.1:g.19808G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262418.12:c.2102G= MANE Select ENSP00000262418.6:p.Gly701=
ENST00000262418.10:c.2102G= ENSP00000262418.6:p.Gly701=
ENST00000399246.3:c.1004G= ENSP00000382190.3:p.Gly335=
NM_000342.3:c.2102G= NP_000333.1:p.Gly701=
XM_005257593.3:c.1907G= XP_005257650.1:p.Gly636=
XM_011525129.1:c.2012G= XP_011523431.1:p.Gly671=
XM_011525130.1:c.2102G= XP_011523432.1:p.Gly701=
XM_005257593.5:c.1907G= XP_005257650.1:p.Gly636=
XM_011525129.2:c.2012G= XP_011523431.1:p.Gly671=
NM_000342.4:c.2102G= MANE Select NP_000333.1:p.Gly701=