Canonical Allele Identifier: CA2261308228
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44254460C= , CM000679.2:g.44254460C= GRCh38
NC_000017.10:g.42331828C= , CM000679.1:g.42331828C= GRCh37
NC_000017.9:g.39687354C= NCBI36
NG_007498.1:g.18675G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.2057+36G= MANE Select ENSP00000262418.6:n.2057+36G=
ENST00000262418.10:c.2057+36G= ENSP00000262418.6:n.2057+36G=
ENST00000399246.3:c.959+36G= ENSP00000382190.3:n.959+36G=
NM_000342.3:c.2057+36G= NP_000333.1:n.2057+36G=
XM_005257593.3:c.1862+36G= XP_005257650.1:n.1862+36G=
XM_011525129.1:c.1967+36G= XP_011523431.1:n.1967+36G=
XM_011525130.1:c.2057+36G= XP_011523432.1:n.2057+36G=
XM_011525131.1:c.2057+36G= XP_011523433.1:n.2057+36G=
XM_005257593.5:c.1862+36G= XP_005257650.1:n.1862+36G=
XM_011525129.2:c.1967+36G= XP_011523431.1:n.1967+36G=
NM_000342.4:c.2057+36G= MANE Select NP_000333.1:n.2057+36G=