Canonical Allele Identifier: CA1425760930

Gene: PARL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183867973A= , CM000665.2:g.183867973A=	GRCh38
NC_000003.11:g.183585761A= , CM000665.1:g.183585761A=	GRCh37
NC_000003.10:g.185068455A=	NCBI36
NG_046164.1:g.21933T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317096.9:c.213T= MANE Select	ENSP00000325421.5:p.Gly71=
ENST00000638817.1:c.213T=	ENSP00000492596.1:p.Gly71=
ENST00000639100.1:c.-481T=	ENSP00000491186.1:n.-481T=
ENST00000639401.1:c.213T=	ENSP00000491227.1:p.Gly71=
ENST00000639900.1:c.213T=	ENSP00000491109.1:p.Gly71=
ENST00000311101.9:c.213T=	ENSP00000310676.5:p.Gly71=
ENST00000317096.8:c.213T=	ENSP00000325421.4:p.Gly71=
ENST00000421484.5:c.213T=	ENSP00000404421.1:p.Gly71=
ENST00000435888.5:c.213T=	ENSP00000402137.1:p.Gly71=
ENST00000449306.1:c.94T=
ENST00000469056.1:n.135T=
NM_001037639.1:c.213T=	NP_001032728.1:p.Gly71=
NM_018622.5:c.213T=	NP_061092.3:p.Gly71=
XM_005247582.3:c.213T=	XP_005247639.1:p.Gly71=
XM_005247584.3:c.213T=	XP_005247641.1:p.Gly71=
NM_001037639.2:c.213T=	NP_001032728.1:p.Gly71=
NM_001324436.1:c.213T=	NP_001311365.1:p.Gly71=
NM_001324437.1:c.213T=	NP_001311366.1:p.Gly71=
NM_001324438.1:c.213T=	NP_001311367.1:p.Gly71=
NM_018622.6:c.213T=	NP_061092.3:p.Gly71=
NR_136893.1:n.275T=
XM_005247582.5:c.213T=	XP_005247639.1:p.Gly71=
XM_017006800.2:c.213T=	XP_016862289.1:p.Gly71=
XM_017006801.1:c.213T=	XP_016862290.1:p.Gly71=
XM_017006802.1:c.213T=	XP_016862291.1:p.Gly71=
XM_017006803.1:c.-417T=	XP_016862292.1:n.-417T=
XM_024453628.1:c.-361T=	XP_024309396.1:n.-361T=
XM_024453630.1:c.-481T=	XP_024309398.1:n.-481T=
XM_024453631.1:c.-537T=	XP_024309399.1:n.-537T=
XM_024453632.1:c.-537T=	XP_024309400.1:n.-537T=
XM_024453633.1:c.-481T=	XP_024309401.1:n.-481T=
NM_001037639.3:c.213T=	NP_001032728.1:p.Gly71=
NM_001324436.2:c.213T=	NP_001311365.1:p.Gly71=
NM_001324437.2:c.213T=	NP_001311366.1:p.Gly71=
NM_001324438.2:c.213T=	NP_001311367.1:p.Gly71=
NM_018622.7:c.213T= MANE Select	NP_061092.3:p.Gly71=
NR_136893.2:n.247T=