Canonical Allele Identifier: CA399782633

Gene: SLC4A1

Linked Data

• gnomAD v4: 17-44254521-T-G
• MyVariant Identifiers: chr17:g.42331889T>G (hg19) ; chr17:g.44254521T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254521T>G , CM000679.2:g.44254521T>G	GRCh38
NC_000017.10:g.42331889T>G , CM000679.1:g.42331889T>G	GRCh37
NC_000017.9:g.39687415T>G	NCBI36
NG_007498.1:g.18614A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262418.12:c.2032A>C MANE Select	ENSP00000262418.6:p.Ile678Leu
ENST00000262418.10:c.2032A>C	ENSP00000262418.6:p.Ile678Leu
ENST00000399246.3:c.934A>C	ENSP00000382190.3:p.Ile312Leu
NM_000342.3:c.2032A>C	NP_000333.1:p.Ile678Leu
XM_005257593.3:c.1837A>C	XP_005257650.1:p.Ile613Leu
XM_011525129.1:c.1942A>C	XP_011523431.1:p.Ile648Leu
XM_011525130.1:c.2032A>C	XP_011523432.1:p.Ile678Leu
XM_011525131.1:c.2032A>C	XP_011523433.1:p.Ile678Leu
XM_005257593.5:c.1837A>C	XP_005257650.1:p.Ile613Leu
XM_011525129.2:c.1942A>C	XP_011523431.1:p.Ile648Leu
NM_000342.4:c.2032A>C MANE Select	NP_000333.1:p.Ile678Leu