Canonical Allele Identifier: CA1884351122

Gene: TPRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137199285G= , CM000671.2:g.137199285G=	GRCh38
NC_000009.11:g.140093737G= , CM000671.1:g.140093737G=	GRCh37
NC_000009.10:g.139213558G=	NCBI36
NG_027801.1:g.6427C=
NG_027801.2:g.9909C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409012.6:c.1427C= MANE Select	ENSP00000387100.4:p.Pro476=
ENST00000333046.8:c.821C=	ENSP00000327617.4:p.Pro274=
ENST00000409012.4:c.1427C=	ENSP00000387100.4:p.Pro476=
ENST00000541945.1:n.90+4819C=
NM_001128228.2:c.1427C=	NP_001121700.2:p.Pro476=
NM_001128228.3:c.1427C= MANE Select	NP_001121700.2:p.Pro476=