Canonical Allele Identifier: CA375776439

Gene: TPRN

Linked Data

• MyVariant Identifiers: chr9:g.140093804G>T (hg19) ; chr9:g.137199352G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137199352G>T , CM000671.2:g.137199352G>T	GRCh38
NC_000009.11:g.140093804G>T , CM000671.1:g.140093804G>T	GRCh37
NC_000009.10:g.139213625G>T	NCBI36
NG_027801.1:g.6360C>A
NG_027801.2:g.9842C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409012.6:c.1360C>A MANE Select	ENSP00000387100.4:p.Pro454Thr
ENST00000333046.8:c.754C>A	ENSP00000327617.4:p.Pro252Thr
ENST00000409012.4:c.1360C>A	ENSP00000387100.4:p.Pro454Thr
ENST00000541945.1:n.90+4752C>A
NM_001128228.2:c.1360C>A	NP_001121700.2:p.Pro454Thr
NM_001128228.3:c.1360C>A MANE Select	NP_001121700.2:p.Pro454Thr