Canonical Allele Identifier: CA2638189688
Gene: SLC4A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44249701C>A , CM000679.2:g.44249701C>A GRCh38
NC_000017.10:g.42327069C>A , CM000679.1:g.42327069C>A GRCh37
NC_000017.9:g.39682595C>A NCBI36
NG_007498.1:g.23434G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.*757G>T MANE Select ENSP00000262418.6:n.*757G>T
ENST00000262418.10:c.*757G>T ENSP00000262418.6:n.*757G>T
ENST00000399246.3:c.*757G>T ENSP00000382190.3:n.*757G>T
ENST00000631130.1:c.-451G>T ENSP00000486787.1:n.-451G>T
NM_000342.3:c.*757G>T NP_000333.1:n.*757G>T
XM_005257593.3:c.*757G>T XP_005257650.1:n.*757G>T
XM_011525129.1:c.*757G>T XP_011523431.1:n.*757G>T
XM_005257593.5:c.*757G>T XP_005257650.1:n.*757G>T
XM_011525129.2:c.*757G>T XP_011523431.1:n.*757G>T
NM_000342.4:c.*757G>T MANE Select NP_000333.1:n.*757G>T