Canonical Allele Identifier: CA2261308070
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44254104A= , CM000679.2:g.44254104A= GRCh38
NC_000017.10:g.42331472A= , CM000679.1:g.42331472A= GRCh37
NC_000017.9:g.39686998A= NCBI36
NG_007498.1:g.19031T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.2057+392T= MANE Select ENSP00000262418.6:n.2057+392T=
ENST00000262418.10:c.2057+392T= ENSP00000262418.6:n.2057+392T=
ENST00000399246.3:c.959+392T= ENSP00000382190.3:n.959+392T=
NM_000342.3:c.2057+392T= NP_000333.1:n.2057+392T=
XM_005257593.3:c.1862+392T= XP_005257650.1:n.1862+392T=
XM_011525129.1:c.1967+392T= XP_011523431.1:n.1967+392T=
XM_011525130.1:c.2057+392T= XP_011523432.1:n.2057+392T=
XM_011525131.1:c.2058-296T= XP_011523433.1:n.2058-296T=
XM_005257593.5:c.1862+392T= XP_005257650.1:n.1862+392T=
XM_011525129.2:c.1967+392T= XP_011523431.1:n.1967+392T=
NM_000342.4:c.2057+392T= MANE Select NP_000333.1:n.2057+392T=