Canonical Allele Identifier: CA2830535965

Gene: PARL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183833995_183833996insC , CM000665.2:g.183833995_183833996insC	GRCh38
NC_000003.11:g.183551783_183551784insC , CM000665.1:g.183551783_183551784insC	GRCh37
NC_000003.10:g.185034477_185034478insC	NCBI36
NG_046164.1:g.55910_55911insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317096.9:c.829-171_829-170insG MANE Select	ENSP00000325421.5:n.829-171_829-170insG
ENST00000638817.1:c.*415-171_*415-170insG	ENSP00000492596.1:n.*415-171_*415-170insG
ENST00000639100.1:c.256-171_256-170insG	ENSP00000491186.1:n.256-171_256-170insG
ENST00000639401.1:c.829-171_829-170insG	ENSP00000491227.1:n.829-171_829-170insG
ENST00000639900.1:c.*483-171_*483-170insG	ENSP00000491109.1:n.*483-171_*483-170insG
ENST00000311101.9:c.679-171_679-170insG	ENSP00000310676.5:n.679-171_679-170insG
ENST00000317096.8:c.829-171_829-170insG	ENSP00000325421.4:n.829-171_829-170insG
ENST00000417784.5:c.203-171_203-170insG
ENST00000418450.5:c.129-407_129-406insG
ENST00000421484.5:c.*363-171_*363-170insG	ENSP00000404421.1:n.*363-171_*363-170insG
ENST00000435888.5:c.679-407_679-406insG	ENSP00000402137.1:n.679-407_679-406insG
ENST00000449306.1:c.419-171_419-170insG
ENST00000450375.5:c.169-4287_169-4286insG	ENSP00000402689.1:n.169-4287_169-4286insG
NM_001037639.1:c.679-171_679-170insG	NP_001032728.1:n.679-171_679-170insG
NM_018622.5:c.829-171_829-170insG	NP_061092.3:n.829-171_829-170insG
XM_005247582.3:c.829-171_829-170insG	XP_005247639.1:n.829-171_829-170insG
XM_005247584.3:c.829-407_829-406insG	XP_005247641.1:n.829-407_829-406insG
XM_005247587.1:c.256-171_256-170insG	XP_005247644.1:n.256-171_256-170insG
NM_001037639.2:c.679-171_679-170insG	NP_001032728.1:n.679-171_679-170insG
NM_001324436.1:c.829-407_829-406insG	NP_001311365.1:n.829-407_829-406insG
NM_001324437.1:c.679-407_679-406insG	NP_001311366.1:n.679-407_679-406insG
NM_001324438.1:c.829-4287_829-4286insG	NP_001311367.1:n.829-4287_829-4286insG
NM_018622.6:c.829-171_829-170insG	NP_061092.3:n.829-171_829-170insG
NR_136893.1:n.947-171_947-170insG
XM_005247582.5:c.829-171_829-170insG	XP_005247639.1:n.829-171_829-170insG
XM_017006800.2:c.829-407_829-406insG	XP_016862289.1:n.829-407_829-406insG
XM_017006801.1:c.679-171_679-170insG	XP_016862290.1:n.679-171_679-170insG
XM_017006802.1:c.679-407_679-406insG	XP_016862291.1:n.679-407_679-406insG
XM_017006803.1:c.106-171_106-170insG	XP_016862292.1:n.106-171_106-170insG
XM_024453628.1:c.256-171_256-170insG	XP_024309396.1:n.256-171_256-170insG
XM_024453629.1:c.256-171_256-170insG	XP_024309397.1:n.256-171_256-170insG
XM_024453630.1:c.256-171_256-170insG	XP_024309398.1:n.256-171_256-170insG
XM_024453631.1:c.256-171_256-170insG	XP_024309399.1:n.256-171_256-170insG
XM_024453632.1:c.256-171_256-170insG	XP_024309400.1:n.256-171_256-170insG
XM_024453633.1:c.256-171_256-170insG	XP_024309401.1:n.256-171_256-170insG
NM_001037639.3:c.679-171_679-170insG	NP_001032728.1:n.679-171_679-170insG
NM_001324436.2:c.829-407_829-406insG	NP_001311365.1:n.829-407_829-406insG
NM_001324437.2:c.679-407_679-406insG	NP_001311366.1:n.679-407_679-406insG
NM_001324438.2:c.829-4287_829-4286insG	NP_001311367.1:n.829-4287_829-4286insG
NM_018622.7:c.829-171_829-170insG MANE Select	NP_061092.3:n.829-171_829-170insG
NR_136893.2:n.919-171_919-170insG