Canonical Allele Identifier: CA768338096

Gene: QPCT

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.37365485C>A , CM000664.2:g.37365485C>A	GRCh38
NC_000002.11:g.37592628C>A , CM000664.1:g.37592628C>A	GRCh37
NC_000002.10:g.37446132C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338415.8:c.547-1747C>A MANE Select	ENSP00000344829.3:n.547-1747C>A
ENST00000650442.1:c.355-1747C>A	ENSP00000498156.1:n.355-1747C>A
ENST00000338415.7:c.547-1747C>A	ENSP00000344829.3:n.547-1747C>A
ENST00000404976.5:c.400-1747C>A	ENSP00000385391.1:n.400-1747C>A
ENST00000480050.1:n.457-1747C>A
NM_012413.3:c.547-1747C>A	NP_036545.1:n.547-1747C>A
NM_012413.4:c.547-1747C>A MANE Select	NP_036545.1:n.547-1747C>A