Canonical Allele Identifier: CA2261306874
Community Standard Title: NM_000342.4(SLC4A1):c.2317T= (p.Ser773=)
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44251583A= , CM000679.2:g.44251583A= GRCh38
NC_000017.10:g.42328951A= , CM000679.1:g.42328951A= GRCh37
NC_000017.9:g.39684477A= NCBI36
NG_007498.1:g.21552T=

Transcript Alleles

HGVS Amino-acid Change
NM_000342.4:c.2317T= MANE Select NP_000333.1:p.Ser773=
ENST00000262418.12:c.2317T= MANE Select ENSP00000262418.6:p.Ser773=
NM_000342.3:c.2317T= NP_000333.1:p.Ser773=
ENST00000262418.10:c.2317T= ENSP00000262418.6:p.Ser773=
ENST00000399246.3:c.1219T= ENSP00000382190.3:p.Ser407=
XM_005257593.3:c.2122T= XP_005257650.1:p.Ser708=
XM_005257593.5:c.2122T= XP_005257650.1:p.Ser708=
XM_011525129.1:c.2227T= XP_011523431.1:p.Ser743=
XM_011525129.2:c.2227T= XP_011523431.1:p.Ser743=
XM_011525130.1:c.*27T= XP_011523432.1:n.*27T=