Canonical Allele Identifier: CA2261306041
Gene: SLC4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44249732C= , CM000679.2:g.44249732C= GRCh38
NC_000017.10:g.42327100C= , CM000679.1:g.42327100C= GRCh37
NC_000017.9:g.39682626C= NCBI36
NG_007498.1:g.23403G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.*726G= MANE Select ENSP00000262418.6:n.*726G=
ENST00000262418.10:c.*726G= ENSP00000262418.6:n.*726G=
ENST00000399246.3:c.*726G= ENSP00000382190.3:n.*726G=
ENST00000631130.1:c.-482G= ENSP00000486787.1:n.-482G=
NM_000342.3:c.*726G= NP_000333.1:n.*726G=
XM_005257593.3:c.*726G= XP_005257650.1:n.*726G=
XM_011525129.1:c.*726G= XP_011523431.1:n.*726G=
XM_005257593.5:c.*726G= XP_005257650.1:n.*726G=
XM_011525129.2:c.*726G= XP_011523431.1:n.*726G=
NM_000342.4:c.*726G= MANE Select NP_000333.1:n.*726G=