Canonical Allele Identifier: CA1884347493

Gene: TPRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137192281T= , CM000671.2:g.137192281T=	GRCh38
NC_000009.11:g.140086733T= , CM000671.1:g.140086733T=	GRCh37
NC_000009.10:g.139206554T=	NCBI36
NG_027801.1:g.13431A=
NG_027801.2:g.16913A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409012.6:c.2051A= MANE Select	ENSP00000387100.4:p.Glu684=
ENST00000333046.8:c.1445A=	ENSP00000327617.4:p.Glu482=
ENST00000409012.4:c.2051A=	ENSP00000387100.4:p.Glu684=
ENST00000477345.1:n.2772A=
NM_001128228.2:c.2051A=	NP_001121700.2:p.Glu684=
NM_001128228.3:c.2051A= MANE Select	NP_001121700.2:p.Glu684=