Canonical Allele Identifier: CA399782549

Gene: SLC4A1

Linked Data

• gnomAD v4: 17-44254502-A-T
• MyVariant Identifiers: chr17:g.42331870A>T (hg19) ; chr17:g.44254502A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254502A>T , CM000679.2:g.44254502A>T	GRCh38
NC_000017.10:g.42331870A>T , CM000679.1:g.42331870A>T	GRCh37
NC_000017.9:g.39687396A>T	NCBI36
NG_007498.1:g.18633T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.2051T>A MANE Select	ENSP00000262418.6:p.Ile684Asn
ENST00000262418.10:c.2051T>A	ENSP00000262418.6:p.Ile684Asn
ENST00000399246.3:c.953T>A	ENSP00000382190.3:p.Ile318Asn
NM_000342.3:c.2051T>A	NP_000333.1:p.Ile684Asn
XM_005257593.3:c.1856T>A	XP_005257650.1:p.Ile619Asn
XM_011525129.1:c.1961T>A	XP_011523431.1:p.Ile654Asn
XM_011525130.1:c.2051T>A	XP_011523432.1:p.Ile684Asn
XM_011525131.1:c.2051T>A	XP_011523433.1:p.Ile684Asn
XM_005257593.5:c.1856T>A	XP_005257650.1:p.Ile619Asn
XM_011525129.2:c.1961T>A	XP_011523431.1:p.Ile654Asn
NM_000342.4:c.2051T>A MANE Select	NP_000333.1:p.Ile684Asn