Canonical Allele Identifier: CA467924931

Gene: TPRN

Linked Data

• dbSNP Id: rs1834758057
• gnomAD v4: 9-137199344-G-A
• MyVariant Identifiers: chr9:g.140093796G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137199344G>A , CM000671.2:g.137199344G>A	GRCh38
NC_000009.11:g.140093796G>A , CM000671.1:g.140093796G>A	GRCh37
NC_000009.10:g.139213617G>A	NCBI36
NG_027801.1:g.6368C>T
NG_027801.2:g.9850C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409012.6:c.1368C>T MANE Select	ENSP00000387100.4:p.Thr456=
ENST00000333046.8:c.762C>T	ENSP00000327617.4:p.Thr254=
ENST00000409012.4:c.1368C>T	ENSP00000387100.4:p.Thr456=
ENST00000541945.1:n.90+4760C>T
NM_001128228.2:c.1368C>T	NP_001121700.2:p.Thr456=
NM_001128228.3:c.1368C>T MANE Select	NP_001121700.2:p.Thr456=