Canonical Allele Identifier: CA2638191250

Gene: SLC4A1

Linked Data

• gnomAD v4: 17-44254469-A-AACCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254469_44254470insACCC , CM000679.2:g.44254469_44254470insACCC	GRCh38
NC_000017.10:g.42331837_42331838insACCC , CM000679.1:g.42331837_42331838insACCC	GRCh37
NC_000017.9:g.39687363_39687364insACCC	NCBI36
NG_007498.1:g.18665_18666insGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.2057+26_2057+27insGGGT MANE Select	ENSP00000262418.6:n.2057+26_2057+27insGGGT
ENST00000262418.10:c.2057+26_2057+27insGGGT	ENSP00000262418.6:n.2057+26_2057+27insGGGT
ENST00000399246.3:c.959+26_959+27insGGGT	ENSP00000382190.3:n.959+26_959+27insGGGT
NM_000342.3:c.2057+26_2057+27insGGGT	NP_000333.1:n.2057+26_2057+27insGGGT
XM_005257593.3:c.1862+26_1862+27insGGGT	XP_005257650.1:n.1862+26_1862+27insGGGT
XM_011525129.1:c.1967+26_1967+27insGGGT	XP_011523431.1:n.1967+26_1967+27insGGGT
XM_011525130.1:c.2057+26_2057+27insGGGT	XP_011523432.1:n.2057+26_2057+27insGGGT
XM_011525131.1:c.2057+26_2057+27insGGGT	XP_011523433.1:n.2057+26_2057+27insGGGT
XM_005257593.5:c.1862+26_1862+27insGGGT	XP_005257650.1:n.1862+26_1862+27insGGGT
XM_011525129.2:c.1967+26_1967+27insGGGT	XP_011523431.1:n.1967+26_1967+27insGGGT
NM_000342.4:c.2057+26_2057+27insGGGT MANE Select	NP_000333.1:n.2057+26_2057+27insGGGT