Canonical Allele Identifier: CA2668769413
Gene: PARL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183867975_183867977del , CM000665.2:g.183867975_183867977del GRCh38
NC_000003.11:g.183585763_183585765del , CM000665.1:g.183585763_183585765del GRCh37
NC_000003.10:g.185068457_185068459del NCBI36
NG_046164.1:g.21932_21934del

Transcript Alleles

HGVS Amino-acid Change
ENST00000317096.9:c.212_214del MANE Select ENSP00000325421.5:p.Gly71del
ENST00000638817.1:c.212_214del ENSP00000492596.1:p.Gly71del
ENST00000639100.1:c.-482_-480del ENSP00000491186.1:n.-482_-480del
ENST00000639401.1:c.212_214del ENSP00000491227.1:p.Gly71del
ENST00000639900.1:c.212_214del ENSP00000491109.1:p.Gly71del
ENST00000311101.9:c.212_214del ENSP00000310676.5:p.Gly71del
ENST00000317096.8:c.212_214del ENSP00000325421.4:p.Gly71del
ENST00000421484.5:c.212_214del ENSP00000404421.1:p.Gly71del
ENST00000435888.5:c.212_214del ENSP00000402137.1:p.Gly71del
ENST00000449306.1:c.93_95del
ENST00000469056.1:n.134_136del
NM_001037639.1:c.212_214del NP_001032728.1:p.Gly71del
NM_018622.5:c.212_214del NP_061092.3:p.Gly71del
XM_005247582.3:c.212_214del XP_005247639.1:p.Gly71del
XM_005247584.3:c.212_214del XP_005247641.1:p.Gly71del
NM_001037639.2:c.212_214del NP_001032728.1:p.Gly71del
NM_001324436.1:c.212_214del NP_001311365.1:p.Gly71del
NM_001324437.1:c.212_214del NP_001311366.1:p.Gly71del
NM_001324438.1:c.212_214del NP_001311367.1:p.Gly71del
NM_018622.6:c.212_214del NP_061092.3:p.Gly71del
NR_136893.1:n.274_276del
XM_005247582.5:c.212_214del XP_005247639.1:p.Gly71del
XM_017006800.2:c.212_214del XP_016862289.1:p.Gly71del
XM_017006801.1:c.212_214del XP_016862290.1:p.Gly71del
XM_017006802.1:c.212_214del XP_016862291.1:p.Gly71del
XM_017006803.1:c.-418_-416del XP_016862292.1:n.-418_-416del
XM_024453628.1:c.-362_-360del XP_024309396.1:n.-362_-360del
XM_024453630.1:c.-482_-480del XP_024309398.1:n.-482_-480del
XM_024453631.1:c.-538_-536del XP_024309399.1:n.-538_-536del
XM_024453632.1:c.-538_-536del XP_024309400.1:n.-538_-536del
XM_024453633.1:c.-482_-480del XP_024309401.1:n.-482_-480del
NM_001037639.3:c.212_214del NP_001032728.1:p.Gly71del
NM_001324436.2:c.212_214del NP_001311365.1:p.Gly71del
NM_001324437.2:c.212_214del NP_001311366.1:p.Gly71del
NM_001324438.2:c.212_214del NP_001311367.1:p.Gly71del
NM_018622.7:c.212_214del MANE Select NP_061092.3:p.Gly71del
NR_136893.2:n.246_248del