Canonical Allele Identifier: CA1884347490
Gene: TPRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137192275G= , CM000671.2:g.137192275G= GRCh38
NC_000009.11:g.140086727G= , CM000671.1:g.140086727G= GRCh37
NC_000009.10:g.139206548G= NCBI36
NG_027801.1:g.13437C=
NG_027801.2:g.16919C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.2057C= MANE Select ENSP00000387100.4:p.Pro686=
ENST00000333046.8:c.1451C= ENSP00000327617.4:p.Pro484=
ENST00000409012.4:c.2057C= ENSP00000387100.4:p.Pro686=
ENST00000477345.1:n.2778C=
NM_001128228.2:c.2057C= NP_001121700.2:p.Pro686=
NM_001128228.3:c.2057C= MANE Select NP_001121700.2:p.Pro686=