Canonical Allele Identifier: CA2261306054
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44249762G= , CM000679.2:g.44249762G= GRCh38
NC_000017.10:g.42327130G= , CM000679.1:g.42327130G= GRCh37
NC_000017.9:g.39682656G= NCBI36
NG_007498.1:g.23373C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.*696C= MANE Select ENSP00000262418.6:n.*696C=
ENST00000262418.10:c.*696C= ENSP00000262418.6:n.*696C=
ENST00000399246.3:c.*696C= ENSP00000382190.3:n.*696C=
ENST00000631130.1:c.-512C= ENSP00000486787.1:n.-512C=
NM_000342.3:c.*696C= NP_000333.1:n.*696C=
XM_005257593.3:c.*696C= XP_005257650.1:n.*696C=
XM_011525129.1:c.*696C= XP_011523431.1:n.*696C=
XM_005257593.5:c.*696C= XP_005257650.1:n.*696C=
XM_011525129.2:c.*696C= XP_011523431.1:n.*696C=
NM_000342.4:c.*696C= MANE Select NP_000333.1:n.*696C=