Canonical Allele Identifier: CA1845834978

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35061506T= , CM000671.2:g.35061506T=	GRCh38
NC_000009.11:g.35061503T= , CM000671.1:g.35061503T=	GRCh37
NC_000009.10:g.35051503T=	NCBI36
NG_007887.1:g.16237A= , LRG_657:g.16237A=

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.1194+71A= MANE Select	NP_009057.1:n.1194+71A=
ENST00000358901.11:c.1194+71A= MANE Select	ENSP00000351777.6:n.1194+71A=
NM_001354927.1:c.1059+71A=	NP_001341856.1:n.1059+71A=
NM_001354927.2:c.1059+71A=	NP_001341856.1:n.1059+71A=
NM_001354928.1:c.1059+71A=	NP_001341857.1:n.1059+71A=
NM_001354928.2:c.1059+71A=	NP_001341857.1:n.1059+71A=
NM_007126.3:c.1194+71A= , LRG_657t1:c.1194+71A=	NP_009057.1:n.1194+71A=
NM_007126.4:c.1194+71A=	NP_009057.1:n.1194+71A=
ENST00000358901.10:c.1194+71A=	ENSP00000351777.6:n.1194+71A=
ENST00000417448.2:c.1059+71A=	ENSP00000399456.2:n.1059+71A=
ENST00000448530.6:c.1059+71A=	ENSP00000392088.2:n.1059+71A=
ENST00000480327.1:n.54+71A=
ENST00000480327.2:n.1332+71A=
ENST00000493886.5:n.1468+71A=
ENST00000676836.2:n.1611A=
ENST00000677257.1:c.1188+71A=	ENSP00000504354.1:n.1188+71A=
ENST00000678018.1:c.*1165+71A=	ENSP00000503811.1:n.*1165+71A=
ENST00000678465.1:c.*206+71A=	ENSP00000504259.1:n.*206+71A=
ENST00000678650.1:c.1059+71A=	ENSP00000503426.1:n.1059+71A=
ENST00000679204.2:c.1194+71A=	ENSP00000503131.2:n.1194+71A=
ENST00000679599.1:n.1464+71A=
ENST00000679647.1:c.1194+71A=	ENSP00000506216.1:n.1194+71A=
ENST00000679800.1:n.1593+71A=
ENST00000679862.1:c.1059+71A=	ENSP00000504990.1:n.1059+71A=
ENST00000679902.1:c.1194+71A=	ENSP00000506338.1:n.1194+71A=
ENST00000680834.1:c.544+71A=
ENST00000680916.1:c.1194+71A=	ENSP00000505769.1:n.1194+71A=
ENST00000681125.1:c.276+71A=
ENST00000681335.1:c.1194+71A=	ENSP00000505230.1:n.1194+71A=
ENST00000681690.1:n.1466+71A=