Canonical Allele Identifier: CA290928598

Gene: SLC4A1

Linked Data

• dbSNP Id: rs769977105
• MyVariant Identifiers: chr17:g.42332011C>T (hg19) ; chr17:g.44254643C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254643C>T , CM000679.2:g.44254643C>T	GRCh38
NC_000017.10:g.42332011C>T , CM000679.1:g.42332011C>T	GRCh37
NC_000017.9:g.39687537C>T	NCBI36
NG_007498.1:g.18492G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.1910G>A MANE Select	ENSP00000262418.6:p.Gly637Asp
ENST00000262418.10:c.1910G>A	ENSP00000262418.6:p.Gly637Asp
ENST00000399246.3:c.812G>A	ENSP00000382190.3:p.Gly271Asp
NM_000342.3:c.1910G>A	NP_000333.1:p.Gly637Asp
XM_005257593.3:c.1715G>A	XP_005257650.1:p.Gly572Asp
XM_011525129.1:c.1820G>A	XP_011523431.1:p.Gly607Asp
XM_011525130.1:c.1910G>A	XP_011523432.1:p.Gly637Asp
XM_011525131.1:c.1910G>A	XP_011523433.1:p.Gly637Asp
XM_005257593.5:c.1715G>A	XP_005257650.1:p.Gly572Asp
XM_011525129.2:c.1820G>A	XP_011523431.1:p.Gly607Asp
NM_000342.4:c.1910G>A MANE Select	NP_000333.1:p.Gly637Asp