Canonical Allele Identifier: CA290924177

Gene: SLC4A1

Linked Data

• dbSNP Id: rs995796367
• MyVariant Identifiers: chr17:g.42327053A>G (hg19) ; chr17:g.44249685A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44249685A>G , CM000679.2:g.44249685A>G	GRCh38
NC_000017.10:g.42327053A>G , CM000679.1:g.42327053A>G	GRCh37
NC_000017.9:g.39682579A>G	NCBI36
NG_007498.1:g.23450T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.*773T>C MANE Select	ENSP00000262418.6:n.*773T>C
ENST00000262418.10:c.*773T>C	ENSP00000262418.6:n.*773T>C
ENST00000399246.3:c.*773T>C	ENSP00000382190.3:n.*773T>C
ENST00000631130.1:c.-435T>C	ENSP00000486787.1:n.-435T>C
NM_000342.3:c.*773T>C	NP_000333.1:n.*773T>C
XM_005257593.3:c.*773T>C	XP_005257650.1:n.*773T>C
XM_011525129.1:c.*773T>C	XP_011523431.1:n.*773T>C
XM_005257593.5:c.*773T>C	XP_005257650.1:n.*773T>C
XM_011525129.2:c.*773T>C	XP_011523431.1:n.*773T>C
NM_000342.4:c.*773T>C MANE Select	NP_000333.1:n.*773T>C