Canonical Allele Identifier: CA2261306025
Gene: SLC4A1 HGNC NCBI

Linked Data

dbSNP Id: rs1047492242

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44249694G>A , CM000679.2:g.44249694G>A GRCh38
NC_000017.10:g.42327062G>A , CM000679.1:g.42327062G>A GRCh37
NC_000017.9:g.39682588G>A NCBI36
NG_007498.1:g.23441C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.*764C>T MANE Select ENSP00000262418.6:n.*764C>T
ENST00000262418.10:c.*764C>T ENSP00000262418.6:n.*764C>T
ENST00000399246.3:c.*764C>T ENSP00000382190.3:n.*764C>T
ENST00000631130.1:c.-444C>T ENSP00000486787.1:n.-444C>T
NM_000342.3:c.*764C>T NP_000333.1:n.*764C>T
XM_005257593.3:c.*764C>T XP_005257650.1:n.*764C>T
XM_011525129.1:c.*764C>T XP_011523431.1:n.*764C>T
XM_005257593.5:c.*764C>T XP_005257650.1:n.*764C>T
XM_011525129.2:c.*764C>T XP_011523431.1:n.*764C>T
NM_000342.4:c.*764C>T MANE Select NP_000333.1:n.*764C>T