Canonical Allele Identifier: CA1884351089

Gene: TPRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137199218G= , CM000671.2:g.137199218G=	GRCh38
NC_000009.11:g.140093670G= , CM000671.1:g.140093670G=	GRCh37
NC_000009.10:g.139213491G=	NCBI36
NG_027801.1:g.6494C=
NG_027801.2:g.9976C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409012.6:c.1494C= MANE Select	ENSP00000387100.4:p.Ser498=
ENST00000333046.8:c.888C=	ENSP00000327617.4:p.Ser296=
ENST00000409012.4:c.1494C=	ENSP00000387100.4:p.Ser498=
ENST00000541945.1:n.90+4886C=
NM_001128228.2:c.1494C=	NP_001121700.2:p.Ser498=
NM_001128228.3:c.1494C= MANE Select	NP_001121700.2:p.Ser498=