Canonical Allele Identifier: CA1884351174

Gene: TPRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137199401C= , CM000671.2:g.137199401C=	GRCh38
NC_000009.11:g.140093853C= , CM000671.1:g.140093853C=	GRCh37
NC_000009.10:g.139213674C=	NCBI36
NG_027801.1:g.6311G=
NG_027801.2:g.9793G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409012.6:c.1311G= MANE Select	ENSP00000387100.4:p.Arg437=
ENST00000333046.8:c.705G=	ENSP00000327617.4:p.Arg235=
ENST00000409012.4:c.1311G=	ENSP00000387100.4:p.Arg437=
ENST00000541945.1:n.90+4703G=
NM_001128228.2:c.1311G=	NP_001121700.2:p.Arg437=
NM_001128228.3:c.1311G= MANE Select	NP_001121700.2:p.Arg437=