Canonical Allele Identifier: CA2638191117

Gene: SLC4A1

Linked Data

• gnomAD v4: 17-44254453-TGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254454_44254456del , CM000679.2:g.44254454_44254456del	GRCh38
NC_000017.10:g.42331822_42331824del , CM000679.1:g.42331822_42331824del	GRCh37
NC_000017.9:g.39687348_39687350del	NCBI36
NG_007498.1:g.18679_18681del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.2057+40_2057+42del MANE Select	ENSP00000262418.6:n.2057+40_2057+42del
ENST00000262418.10:c.2057+40_2057+42del	ENSP00000262418.6:n.2057+40_2057+42del
ENST00000399246.3:c.959+40_959+42del	ENSP00000382190.3:n.959+40_959+42del
NM_000342.3:c.2057+40_2057+42del	NP_000333.1:n.2057+40_2057+42del
XM_005257593.3:c.1862+40_1862+42del	XP_005257650.1:n.1862+40_1862+42del
XM_011525129.1:c.1967+40_1967+42del	XP_011523431.1:n.1967+40_1967+42del
XM_011525130.1:c.2057+40_2057+42del	XP_011523432.1:n.2057+40_2057+42del
XM_011525131.1:c.2057+40_2057+42del	XP_011523433.1:n.2057+40_2057+42del
XM_005257593.5:c.1862+40_1862+42del	XP_005257650.1:n.1862+40_1862+42del
XM_011525129.2:c.1967+40_1967+42del	XP_011523431.1:n.1967+40_1967+42del
NM_000342.4:c.2057+40_2057+42del MANE Select	NP_000333.1:n.2057+40_2057+42del