Canonical Allele Identifier: CA2261308604
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44255292C= , CM000679.2:g.44255292C= GRCh38
NC_000017.10:g.42332660C= , CM000679.1:g.42332660C= GRCh37
NC_000017.9:g.39688186C= NCBI36
NG_007498.1:g.17843G=

Transcript Alleles

HGVS Amino-acid Change
NM_000342.4:c.1805G= MANE Select NP_000333.1:p.Arg602=
ENST00000262418.12:c.1805G= MANE Select ENSP00000262418.6:p.Arg602=
NM_000342.3:c.1805G= NP_000333.1:p.Arg602=
ENST00000262418.10:c.1805G= ENSP00000262418.6:p.Arg602=
ENST00000399246.3:c.778-71G= ENSP00000382190.3:n.778-71G=
XM_005257593.3:c.1610G= XP_005257650.1:p.Arg537=
XM_005257593.5:c.1610G= XP_005257650.1:p.Arg537=
XM_011525129.1:c.1800+381G= XP_011523431.1:n.1800+381G=
XM_011525129.2:c.1800+381G= XP_011523431.1:n.1800+381G=
XM_011525130.1:c.1805G= XP_011523432.1:p.Arg602=
XM_011525131.1:c.1805G= XP_011523433.1:p.Arg602=