Canonical Allele Identifier: CA399794233

Gene: SLC4A1

Linked Data

• ClinVar Variation Id: 544806
• ClinVar RCV Id: RCV000655903
• dbSNP Id: rs1555596757
• MyVariant Identifiers: chr17:g.42337302T>C (hg19) ; chr17:g.44259934T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44259934T>C , CM000679.2:g.44259934T>C	GRCh38
NC_000017.10:g.42337302T>C , CM000679.1:g.42337302T>C	GRCh37
NC_000017.9:g.39692828T>C	NCBI36
NG_007498.1:g.13201A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.486-2A>G MANE Select	ENSP00000262418.6:n.486-2A>G
ENST00000262418.10:c.486-2A>G	ENSP00000262418.6:n.486-2A>G
ENST00000399246.3:c.486-2A>G	ENSP00000382190.3:n.486-2A>G
ENST00000497360.5:n.625-2A>G
NM_000342.3:c.486-2A>G	NP_000333.1:n.486-2A>G
XM_005257593.3:c.291-2A>G	XP_005257650.1:n.291-2A>G
XM_011525129.1:c.486-2A>G	XP_011523431.1:n.486-2A>G
XM_011525130.1:c.486-2A>G	XP_011523432.1:n.486-2A>G
XM_011525131.1:c.486-2A>G	XP_011523433.1:n.486-2A>G
XM_005257593.5:c.291-2A>G	XP_005257650.1:n.291-2A>G
XM_011525129.2:c.486-2A>G	XP_011523431.1:n.486-2A>G
NM_000342.4:c.486-2A>G MANE Select	NP_000333.1:n.486-2A>G