Canonical Allele Identifier: CA2667251756

Gene: PARP15

Linked Data

• gnomAD v4: 3-122610357-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122610357C>A , CM000665.2:g.122610357C>A	GRCh38
NC_000003.11:g.122329204C>A , CM000665.1:g.122329204C>A	GRCh37
NC_000003.10:g.123811894C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000464300.7:c.307-137C>A MANE Select	ENSP00000417214.2:n.307-137C>A
ENST00000464300.6:c.307-137C>A	ENSP00000417214.2:n.307-137C>A
ENST00000465304.5:n.283-137C>A
ENST00000483793.5:c.307-137C>A	ENSP00000417785.1:n.307-137C>A
NM_001113523.1:c.307-137C>A	NP_001106995.1:n.307-137C>A
NM_001113523.2:c.307-137C>A	NP_001106995.1:n.307-137C>A
NM_001308320.1:c.307-137C>A	NP_001295249.1:n.307-137C>A
XM_005247159.2:c.307-137C>A	XP_005247216.1:n.307-137C>A
XM_005247160.2:c.307-137C>A	XP_005247217.1:n.307-137C>A
XM_011512475.1:c.187-137C>A	XP_011510777.1:n.187-137C>A
XM_011512476.1:c.307-137C>A	XP_011510778.1:n.307-137C>A
XM_011512477.1:c.307-137C>A	XP_011510779.1:n.307-137C>A
XM_011512478.1:c.-488-137C>A	XP_011510780.1:n.-488-137C>A
XM_011512480.1:c.307-137C>A	XP_011510782.1:n.307-137C>A
XM_005247159.4:c.307-137C>A	XP_005247216.1:n.307-137C>A
XM_005247160.4:c.307-137C>A	XP_005247217.1:n.307-137C>A
XM_011512475.3:c.187-137C>A	XP_011510777.1:n.187-137C>A
XM_011512476.3:c.307-137C>A	XP_011510778.1:n.307-137C>A
XM_011512477.3:c.307-137C>A	XP_011510779.1:n.307-137C>A
XM_011512478.3:c.-488-137C>A	XP_011510780.1:n.-488-137C>A
XM_011512480.3:c.307-137C>A	XP_011510782.1:n.307-137C>A
XM_017005791.2:c.307-137C>A	XP_016861280.1:n.307-137C>A
NM_001113523.3:c.307-137C>A MANE Select	NP_001106995.1:n.307-137C>A
NM_001308320.2:c.307-137C>A	NP_001295249.1:n.307-137C>A