Canonical Allele Identifier: CA2216883946

Gene: PRSS53

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31087690T= , CM000678.2:g.31087690T=	GRCh38
NC_000016.9:g.31099011T= , CM000678.1:g.31099011T=	GRCh37
NC_000016.8:g.31006512T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001039503.3:c.89A= MANE Select	NP_001034592.1:p.Gln30=
ENST00000280606.7:c.89A= MANE Select	ENSP00000280606.6:p.Gln30=
NM_001039503.2:c.89A=	NP_001034592.1:p.Gln30=
ENST00000280606.6:c.89A=	ENSP00000280606.6:p.Gln30=
ENST00000486499.1:n.1939A=
ENST00000492427.2:n.1039A=
ENST00000529564.1:c.314A=	ENSP00000431371.1:p.Gln105=
ENST00000532364.1:c.174-792A=	ENSP00000460316.1:n.174-792A=
ENST00000533518.5:c.438A=
XM_011545816.1:c.89A=	XP_011544118.1:p.Gln30=
XM_011545816.2:c.89A=	XP_011544118.1:p.Gln30=
XM_011545817.1:c.89A=	XP_011544119.1:p.Gln30=
XM_011545817.2:c.89A=	XP_011544119.1:p.Gln30=
XM_011545818.1:c.89A=	XP_011544120.1:p.Gln30=
XM_011545818.3:c.89A=	XP_011544120.1:p.Gln30=
XM_011545819.1:c.89A=	XP_011544121.1:p.Gln30=
XM_011545819.2:c.89A=	XP_011544121.1:p.Gln30=
XM_011545820.1:c.89A=	XP_011544122.1:p.Gln30=
XM_011545820.2:c.89A=	XP_011544122.1:p.Gln30=