Canonical Allele Identifier: CA2261310928
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44260501C= , CM000679.2:g.44260501C= GRCh38
NC_000017.10:g.42337869C= , CM000679.1:g.42337869C= GRCh37
NC_000017.9:g.39693395C= NCBI36
NG_007498.1:g.12634G=

Transcript Alleles

HGVS Amino-acid Change
NM_000342.4:c.388G= MANE Select NP_000333.1:p.Gly130=
ENST00000262418.12:c.388G= MANE Select ENSP00000262418.6:p.Gly130=
NM_000342.3:c.388G= NP_000333.1:p.Gly130=
ENST00000262418.10:c.388G= ENSP00000262418.6:p.Gly130=
ENST00000399246.3:c.388G= ENSP00000382190.3:p.Gly130=
ENST00000471005.5:n.322G=
ENST00000497360.5:n.527G=
XM_005257593.3:c.193G= XP_005257650.1:p.Gly65=
XM_005257593.5:c.193G= XP_005257650.1:p.Gly65=
XM_011525129.1:c.388G= XP_011523431.1:p.Gly130=
XM_011525129.2:c.388G= XP_011523431.1:p.Gly130=
XM_011525130.1:c.388G= XP_011523432.1:p.Gly130=
XM_011525131.1:c.388G= XP_011523433.1:p.Gly130=