Canonical Allele Identifier: CA2261305691
Gene: SLC4A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44248976C= , CM000679.2:g.44248976C= GRCh38
NC_000017.10:g.42326344C= , CM000679.1:g.42326344C= GRCh37
NC_000017.9:g.39681870C= NCBI36
NG_007498.1:g.24159G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.*1482G= MANE Select ENSP00000262418.6:n.*1482G=
ENST00000262418.10:c.*1482G= ENSP00000262418.6:n.*1482G=
ENST00000399246.3:c.*1482G= ENSP00000382190.3:n.*1482G=
ENST00000631130.1:c.*118G= ENSP00000486787.1:n.*118G=
NM_000342.3:c.*1482G= NP_000333.1:n.*1482G=
XM_005257593.3:c.*1482G= XP_005257650.1:n.*1482G=
XM_011525129.1:c.*1482G= XP_011523431.1:n.*1482G=
NM_000342.4:c.*1482G= MANE Select NP_000333.1:n.*1482G=
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