Canonical Allele Identifier: CA1884351168
Gene: TPRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199379T= , CM000671.2:g.137199379T= GRCh38
NC_000009.11:g.140093831T= , CM000671.1:g.140093831T= GRCh37
NC_000009.10:g.139213652T= NCBI36
NG_027801.1:g.6333A=
NG_027801.2:g.9815A=

Transcript Alleles

HGVS Amino-acid change
ENST00000409012.6:c.1333A= MANE Select ENSP00000387100.4:p.Ser445=
ENST00000333046.8:c.727A= ENSP00000327617.4:p.Ser243=
ENST00000409012.4:c.1333A= ENSP00000387100.4:p.Ser445=
ENST00000541945.1:n.90+4725A=
NM_001128228.2:c.1333A= NP_001121700.2:p.Ser445=
NM_001128228.3:c.1333A= MANE Select NP_001121700.2:p.Ser445=