Canonical Allele Identifier: CA2261306042

Gene: SLC4A1

Linked Data

• dbSNP Id: rs1683830045
• gnomAD v4: 17-44249732-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44249732C>T , CM000679.2:g.44249732C>T	GRCh38
NC_000017.10:g.42327100C>T , CM000679.1:g.42327100C>T	GRCh37
NC_000017.9:g.39682626C>T	NCBI36
NG_007498.1:g.23403G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.*726G>A MANE Select	ENSP00000262418.6:n.*726G>A
ENST00000262418.10:c.*726G>A	ENSP00000262418.6:n.*726G>A
ENST00000399246.3:c.*726G>A	ENSP00000382190.3:n.*726G>A
ENST00000631130.1:c.-482G>A	ENSP00000486787.1:n.-482G>A
NM_000342.3:c.*726G>A	NP_000333.1:n.*726G>A
XM_005257593.3:c.*726G>A	XP_005257650.1:n.*726G>A
XM_011525129.1:c.*726G>A	XP_011523431.1:n.*726G>A
XM_005257593.5:c.*726G>A	XP_005257650.1:n.*726G>A
XM_011525129.2:c.*726G>A	XP_011523431.1:n.*726G>A
NM_000342.4:c.*726G>A MANE Select	NP_000333.1:n.*726G>A