Canonical Allele Identifier: CA338167124

Gene: PARK7

Linked Data

• MyVariant Identifiers: chr1:g.7984956_7984958del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7984956_7984958del , CM000663.2:g.7984956_7984958del	GRCh38
NC_000001.10:g.8045016_8045018del , CM000663.1:g.8045016_8045018del	GRCh37
NC_000001.9:g.7967603_7967605del	NCBI36
NG_008271.1:g.28303_28305del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338639.10:c.472_474del MANE Select	ENSP00000340278.5:p.Pro158del
ENST00000338639.9:c.472_474del	ENSP00000340278.5:p.Pro158del
ENST00000377488.5:c.472_474del	ENSP00000366708.1:p.Pro158del
ENST00000377491.5:c.472_474del	ENSP00000366711.1:p.Pro158del
ENST00000377493.9:c.412_414del	ENSP00000466242.1:p.Pro138del
ENST00000469225.1:c.385_387del	ENSP00000466756.1:p.Pro129del
ENST00000493373.5:c.472_474del	ENSP00000465404.1:p.Pro158del
ENST00000493678.5:c.472_474del	ENSP00000418770.1:p.Pro158del
NM_001123377.1:c.472_474del	NP_001116849.1:p.Pro158del
NM_007262.4:c.472_474del	NP_009193.2:p.Pro158del
XM_005263424.2:c.472_474del	XP_005263481.1:p.Pro158del
XM_005263424.3:c.472_474del	XP_005263481.1:p.Pro158del
NM_007262.5:c.472_474del MANE Select	NP_009193.2:p.Pro158del
NM_001123377.2:c.472_474del	NP_001116849.1:p.Pro158del