Canonical Allele Identifier: CA2638191213

Gene: SLC4A1

Linked Data

• gnomAD v4: 17-44254463-CCTCCCAGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254465_44254472del , CM000679.2:g.44254465_44254472del	GRCh38
NC_000017.10:g.42331833_42331840del , CM000679.1:g.42331833_42331840del	GRCh37
NC_000017.9:g.39687359_39687366del	NCBI36
NG_007498.1:g.18664_18671del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.2057+25_2057+32del MANE Select	ENSP00000262418.6:n.2057+25_2057+32del
ENST00000262418.10:c.2057+25_2057+32del	ENSP00000262418.6:n.2057+25_2057+32del
ENST00000399246.3:c.959+25_959+32del	ENSP00000382190.3:n.959+25_959+32del
NM_000342.3:c.2057+25_2057+32del	NP_000333.1:n.2057+25_2057+32del
XM_005257593.3:c.1862+25_1862+32del	XP_005257650.1:n.1862+25_1862+32del
XM_011525129.1:c.1967+25_1967+32del	XP_011523431.1:n.1967+25_1967+32del
XM_011525130.1:c.2057+25_2057+32del	XP_011523432.1:n.2057+25_2057+32del
XM_011525131.1:c.2057+25_2057+32del	XP_011523433.1:n.2057+25_2057+32del
XM_005257593.5:c.1862+25_1862+32del	XP_005257650.1:n.1862+25_1862+32del
XM_011525129.2:c.1967+25_1967+32del	XP_011523431.1:n.1967+25_1967+32del
NM_000342.4:c.2057+25_2057+32del MANE Select	NP_000333.1:n.2057+25_2057+32del