Canonical Allele Identifier: CA1884351117

Gene: TPRN

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137199278A= , CM000671.2:g.137199278A=	GRCh38
NC_000009.11:g.140093730A= , CM000671.1:g.140093730A=	GRCh37
NC_000009.10:g.139213551A=	NCBI36
NG_027801.1:g.6434T=
NG_027801.2:g.9916T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409012.6:c.1434T= MANE Select	ENSP00000387100.4:p.Pro478=
ENST00000333046.8:c.828T=	ENSP00000327617.4:p.Pro276=
ENST00000409012.4:c.1434T=	ENSP00000387100.4:p.Pro478=
ENST00000541945.1:n.90+4826T=
NM_001128228.2:c.1434T=	NP_001121700.2:p.Pro478=
NM_001128228.3:c.1434T= MANE Select	NP_001121700.2:p.Pro478=