Canonical Allele Identifier: CA1425760944

Gene: PARL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183868002G= , CM000665.2:g.183868002G=	GRCh38
NC_000003.11:g.183585790G= , CM000665.1:g.183585790G=	GRCh37
NC_000003.10:g.185068484G=	NCBI36
NG_046164.1:g.21904C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317096.9:c.184C= MANE Select	ENSP00000325421.5:p.Pro62=
ENST00000638817.1:c.184C=	ENSP00000492596.1:p.Pro62=
ENST00000639100.1:c.-510C=	ENSP00000491186.1:n.-510C=
ENST00000639401.1:c.184C=	ENSP00000491227.1:p.Pro62=
ENST00000639900.1:c.184C=	ENSP00000491109.1:p.Pro62=
ENST00000311101.9:c.184C=	ENSP00000310676.5:p.Pro62=
ENST00000317096.8:c.184C=	ENSP00000325421.4:p.Pro62=
ENST00000421484.5:c.184C=	ENSP00000404421.1:p.Pro62=
ENST00000435888.5:c.184C=	ENSP00000402137.1:p.Pro62=
ENST00000449306.1:c.65C=
ENST00000469056.1:n.106C=
NM_001037639.1:c.184C=	NP_001032728.1:p.Pro62=
NM_018622.5:c.184C=	NP_061092.3:p.Pro62=
XM_005247582.3:c.184C=	XP_005247639.1:p.Pro62=
XM_005247584.3:c.184C=	XP_005247641.1:p.Pro62=
NM_001037639.2:c.184C=	NP_001032728.1:p.Pro62=
NM_001324436.1:c.184C=	NP_001311365.1:p.Pro62=
NM_001324437.1:c.184C=	NP_001311366.1:p.Pro62=
NM_001324438.1:c.184C=	NP_001311367.1:p.Pro62=
NM_018622.6:c.184C=	NP_061092.3:p.Pro62=
NR_136893.1:n.246C=
XM_005247582.5:c.184C=	XP_005247639.1:p.Pro62=
XM_017006800.2:c.184C=	XP_016862289.1:p.Pro62=
XM_017006801.1:c.184C=	XP_016862290.1:p.Pro62=
XM_017006802.1:c.184C=	XP_016862291.1:p.Pro62=
XM_017006803.1:c.-446C=	XP_016862292.1:n.-446C=
XM_024453628.1:c.-390C=	XP_024309396.1:n.-390C=
XM_024453630.1:c.-510C=	XP_024309398.1:n.-510C=
XM_024453631.1:c.-566C=	XP_024309399.1:n.-566C=
XM_024453632.1:c.-566C=	XP_024309400.1:n.-566C=
XM_024453633.1:c.-510C=	XP_024309401.1:n.-510C=
NM_001037639.3:c.184C=	NP_001032728.1:p.Pro62=
NM_001324436.2:c.184C=	NP_001311365.1:p.Pro62=
NM_001324437.2:c.184C=	NP_001311366.1:p.Pro62=
NM_001324438.2:c.184C=	NP_001311367.1:p.Pro62=
NM_018622.7:c.184C= MANE Select	NP_061092.3:p.Pro62=
NR_136893.2:n.218C=