Canonical Allele Identifier: CA2261308251
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44254498G= , CM000679.2:g.44254498G= GRCh38
NC_000017.10:g.42331866G= , CM000679.1:g.42331866G= GRCh37
NC_000017.9:g.39687392G= NCBI36
NG_007498.1:g.18637C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.2055C= MANE Select ENSP00000262418.6:p.Thr685=
ENST00000262418.10:c.2055C= ENSP00000262418.6:p.Thr685=
ENST00000399246.3:c.957C= ENSP00000382190.3:p.Thr319=
NM_000342.3:c.2055C= NP_000333.1:p.Thr685=
XM_005257593.3:c.1860C= XP_005257650.1:p.Thr620=
XM_011525129.1:c.1965C= XP_011523431.1:p.Thr655=
XM_011525130.1:c.2055C= XP_011523432.1:p.Thr685=
XM_011525131.1:c.2055C= XP_011523433.1:p.Thr685=
XM_005257593.5:c.1860C= XP_005257650.1:p.Thr620=
XM_011525129.2:c.1965C= XP_011523431.1:p.Thr655=
NM_000342.4:c.2055C= MANE Select NP_000333.1:p.Thr685=