Canonical Allele Identifier: CA2638191118

Gene: SLC4A1

Linked Data

• gnomAD v4: 17-44254453-T-TGCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254456_44254457insAGCC , CM000679.2:g.44254456_44254457insAGCC	GRCh38
NC_000017.10:g.42331824_42331825insAGCC , CM000679.1:g.42331824_42331825insAGCC	GRCh37
NC_000017.9:g.39687350_39687351insAGCC	NCBI36
NG_007498.1:g.18681_18682insTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.2057+42_2057+43insTGGC MANE Select	ENSP00000262418.6:n.2057+42_2057+43insTGGC
ENST00000262418.10:c.2057+42_2057+43insTGGC	ENSP00000262418.6:n.2057+42_2057+43insTGGC
ENST00000399246.3:c.959+42_959+43insTGGC	ENSP00000382190.3:n.959+42_959+43insTGGC
NM_000342.3:c.2057+42_2057+43insTGGC	NP_000333.1:n.2057+42_2057+43insTGGC
XM_005257593.3:c.1862+42_1862+43insTGGC	XP_005257650.1:n.1862+42_1862+43insTGGC
XM_011525129.1:c.1967+42_1967+43insTGGC	XP_011523431.1:n.1967+42_1967+43insTGGC
XM_011525130.1:c.2057+42_2057+43insTGGC	XP_011523432.1:n.2057+42_2057+43insTGGC
XM_011525131.1:c.2057+42_2057+43insTGGC	XP_011523433.1:n.2057+42_2057+43insTGGC
XM_005257593.5:c.1862+42_1862+43insTGGC	XP_005257650.1:n.1862+42_1862+43insTGGC
XM_011525129.2:c.1967+42_1967+43insTGGC	XP_011523431.1:n.1967+42_1967+43insTGGC
NM_000342.4:c.2057+42_2057+43insTGGC MANE Select	NP_000333.1:n.2057+42_2057+43insTGGC