Canonical Allele Identifier: CA2261307713
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44253332G= , CM000679.2:g.44253332G= GRCh38
NC_000017.10:g.42330700G= , CM000679.1:g.42330700G= GRCh37
NC_000017.9:g.39686226G= NCBI36
NG_007498.1:g.19803C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262418.12:c.2097C= MANE Select ENSP00000262418.6:p.Gly699=
ENST00000262418.10:c.2097C= ENSP00000262418.6:p.Gly699=
ENST00000399246.3:c.999C= ENSP00000382190.3:p.Gly333=
NM_000342.3:c.2097C= NP_000333.1:p.Gly699=
XM_005257593.3:c.1902C= XP_005257650.1:p.Gly634=
XM_011525129.1:c.2007C= XP_011523431.1:p.Gly669=
XM_011525130.1:c.2097C= XP_011523432.1:p.Gly699=
XM_005257593.5:c.1902C= XP_005257650.1:p.Gly634=
XM_011525129.2:c.2007C= XP_011523431.1:p.Gly669=
NM_000342.4:c.2097C= MANE Select NP_000333.1:p.Gly699=