Canonical Allele Identifier: CA2261308302
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44254653C= , CM000679.2:g.44254653C= GRCh38
NC_000017.10:g.42332021C= , CM000679.1:g.42332021C= GRCh37
NC_000017.9:g.39687547C= NCBI36
NG_007498.1:g.18482G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.1900G= MANE Select ENSP00000262418.6:p.Val634=
ENST00000262418.10:c.1900G= ENSP00000262418.6:p.Val634=
ENST00000399246.3:c.802G= ENSP00000382190.3:p.Val268=
NM_000342.3:c.1900G= NP_000333.1:p.Val634=
XM_005257593.3:c.1705G= XP_005257650.1:p.Val569=
XM_011525129.1:c.1810G= XP_011523431.1:p.Val604=
XM_011525130.1:c.1900G= XP_011523432.1:p.Val634=
XM_011525131.1:c.1900G= XP_011523433.1:p.Val634=
XM_005257593.5:c.1705G= XP_005257650.1:p.Val569=
XM_011525129.2:c.1810G= XP_011523431.1:p.Val604=
NM_000342.4:c.1900G= MANE Select NP_000333.1:p.Val634=