Canonical Allele Identifier: CA1884351098

Gene: TPRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137199240G= , CM000671.2:g.137199240G=	GRCh38
NC_000009.11:g.140093692G= , CM000671.1:g.140093692G=	GRCh37
NC_000009.10:g.139213513G=	NCBI36
NG_027801.1:g.6472C=
NG_027801.2:g.9954C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409012.6:c.1472C= MANE Select	ENSP00000387100.4:p.Ala491=
ENST00000333046.8:c.866C=	ENSP00000327617.4:p.Ala289=
ENST00000409012.4:c.1472C=	ENSP00000387100.4:p.Ala491=
ENST00000541945.1:n.90+4864C=
NM_001128228.2:c.1472C=	NP_001121700.2:p.Ala491=
NM_001128228.3:c.1472C= MANE Select	NP_001121700.2:p.Ala491=