Canonical Allele Identifier: CA399777380
Gene: SLC4A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42326464A>T (hg19) chr17:g.44249096A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44249096A>T , CM000679.2:g.44249096A>T GRCh38
NC_000017.10:g.42326464A>T , CM000679.1:g.42326464A>T GRCh37
NC_000017.9:g.39681990A>T NCBI36
NG_007498.1:g.24039T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262418.12:c.*1362T>A MANE Select ENSP00000262418.6:n.*1362T>A
ENST00000262418.10:c.*1362T>A ENSP00000262418.6:n.*1362T>A
ENST00000399246.3:c.*1362T>A ENSP00000382190.3:n.*1362T>A
ENST00000631130.1:c.109T>A ENSP00000486787.1:p.Ter37Arg
NM_000342.3:c.*1362T>A NP_000333.1:n.*1362T>A
XM_005257593.3:c.*1362T>A XP_005257650.1:n.*1362T>A
XM_011525129.1:c.*1362T>A XP_011523431.1:n.*1362T>A
NM_000342.4:c.*1362T>A MANE Select NP_000333.1:n.*1362T>A
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