Canonical Allele Identifier: CA399783411
Gene: SLC4A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44254629T>A , CM000679.2:g.44254629T>A GRCh38
NC_000017.10:g.42331997T>A , CM000679.1:g.42331997T>A GRCh37
NC_000017.9:g.39687523T>A NCBI36
NG_007498.1:g.18506A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262418.12:c.1924A>T MANE Select ENSP00000262418.6:p.Asn642Tyr
ENST00000262418.10:c.1924A>T ENSP00000262418.6:p.Asn642Tyr
ENST00000399246.3:c.826A>T ENSP00000382190.3:p.Asn276Tyr
NM_000342.3:c.1924A>T NP_000333.1:p.Asn642Tyr
XM_005257593.3:c.1729A>T XP_005257650.1:p.Asn577Tyr
XM_011525129.1:c.1834A>T XP_011523431.1:p.Asn612Tyr
XM_011525130.1:c.1924A>T XP_011523432.1:p.Asn642Tyr
XM_011525131.1:c.1924A>T XP_011523433.1:p.Asn642Tyr
XM_005257593.5:c.1729A>T XP_005257650.1:p.Asn577Tyr
XM_011525129.2:c.1834A>T XP_011523431.1:p.Asn612Tyr
NM_000342.4:c.1924A>T MANE Select NP_000333.1:p.Asn642Tyr