Canonical Allele Identifier: CA1884351219
Gene: TPRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199486C= , CM000671.2:g.137199486C= GRCh38
NC_000009.11:g.140093938C= , CM000671.1:g.140093938C= GRCh37
NC_000009.10:g.139213759C= NCBI36
NG_027801.1:g.6226G=
NG_027801.2:g.9708G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1226G= MANE Select ENSP00000387100.4:p.Arg409=
ENST00000333046.8:c.620G= ENSP00000327617.4:p.Arg207=
ENST00000409012.4:c.1226G= ENSP00000387100.4:p.Arg409=
ENST00000541945.1:n.90+4618G=
NM_001128228.2:c.1226G= NP_001121700.2:p.Arg409=
NM_001128228.3:c.1226G= MANE Select NP_001121700.2:p.Arg409=