Canonical Allele Identifier: CA399783141
Gene: SLC4A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44254601T>A , CM000679.2:g.44254601T>A GRCh38
NC_000017.10:g.42331969T>A , CM000679.1:g.42331969T>A GRCh37
NC_000017.9:g.39687495T>A NCBI36
NG_007498.1:g.18534A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.1952A>T MANE Select ENSP00000262418.6:p.His651Leu
ENST00000262418.10:c.1952A>T ENSP00000262418.6:p.His651Leu
ENST00000399246.3:c.854A>T ENSP00000382190.3:p.His285Leu
NM_000342.3:c.1952A>T NP_000333.1:p.His651Leu
XM_005257593.3:c.1757A>T XP_005257650.1:p.His586Leu
XM_011525129.1:c.1862A>T XP_011523431.1:p.His621Leu
XM_011525130.1:c.1952A>T XP_011523432.1:p.His651Leu
XM_011525131.1:c.1952A>T XP_011523433.1:p.His651Leu
XM_005257593.5:c.1757A>T XP_005257650.1:p.His586Leu
XM_011525129.2:c.1862A>T XP_011523431.1:p.His621Leu
NM_000342.4:c.1952A>T MANE Select NP_000333.1:p.His651Leu