Canonical Allele Identifier: CA2638191238

Gene: SLC4A1

Linked Data

• gnomAD v4: 17-44254467-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254468_44254469del , CM000679.2:g.44254468_44254469del	GRCh38
NC_000017.10:g.42331836_42331837del , CM000679.1:g.42331836_42331837del	GRCh37
NC_000017.9:g.39687362_39687363del	NCBI36
NG_007498.1:g.18666_18667del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.2057+27_2057+28del MANE Select	ENSP00000262418.6:n.2057+27_2057+28del
ENST00000262418.10:c.2057+27_2057+28del	ENSP00000262418.6:n.2057+27_2057+28del
ENST00000399246.3:c.959+27_959+28del	ENSP00000382190.3:n.959+27_959+28del
NM_000342.3:c.2057+27_2057+28del	NP_000333.1:n.2057+27_2057+28del
XM_005257593.3:c.1862+27_1862+28del	XP_005257650.1:n.1862+27_1862+28del
XM_011525129.1:c.1967+27_1967+28del	XP_011523431.1:n.1967+27_1967+28del
XM_011525130.1:c.2057+27_2057+28del	XP_011523432.1:n.2057+27_2057+28del
XM_011525131.1:c.2057+27_2057+28del	XP_011523433.1:n.2057+27_2057+28del
XM_005257593.5:c.1862+27_1862+28del	XP_005257650.1:n.1862+27_1862+28del
XM_011525129.2:c.1967+27_1967+28del	XP_011523431.1:n.1967+27_1967+28del
NM_000342.4:c.2057+27_2057+28del MANE Select	NP_000333.1:n.2057+27_2057+28del