Canonical Allele Identifier: CA2638191272

Gene: SLC4A1

Linked Data

• gnomAD v4: 17-44254475-A-ACCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254475_44254476insCCCC , CM000679.2:g.44254475_44254476insCCCC	GRCh38
NC_000017.10:g.42331843_42331844insCCCC , CM000679.1:g.42331843_42331844insCCCC	GRCh37
NC_000017.9:g.39687369_39687370insCCCC	NCBI36
NG_007498.1:g.18659_18660insGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.2057+20_2057+21insGGGG MANE Select	ENSP00000262418.6:n.2057+20_2057+21insGGGG
ENST00000262418.10:c.2057+20_2057+21insGGGG	ENSP00000262418.6:n.2057+20_2057+21insGGGG
ENST00000399246.3:c.959+20_959+21insGGGG	ENSP00000382190.3:n.959+20_959+21insGGGG
NM_000342.3:c.2057+20_2057+21insGGGG	NP_000333.1:n.2057+20_2057+21insGGGG
XM_005257593.3:c.1862+20_1862+21insGGGG	XP_005257650.1:n.1862+20_1862+21insGGGG
XM_011525129.1:c.1967+20_1967+21insGGGG	XP_011523431.1:n.1967+20_1967+21insGGGG
XM_011525130.1:c.2057+20_2057+21insGGGG	XP_011523432.1:n.2057+20_2057+21insGGGG
XM_011525131.1:c.2057+20_2057+21insGGGG	XP_011523433.1:n.2057+20_2057+21insGGGG
XM_005257593.5:c.1862+20_1862+21insGGGG	XP_005257650.1:n.1862+20_1862+21insGGGG
XM_011525129.2:c.1967+20_1967+21insGGGG	XP_011523431.1:n.1967+20_1967+21insGGGG
NM_000342.4:c.2057+20_2057+21insGGGG MANE Select	NP_000333.1:n.2057+20_2057+21insGGGG