Canonical Allele Identifier: CA375776839
Gene: TPRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199415C>A , CM000671.2:g.137199415C>A GRCh38
NC_000009.11:g.140093867C>A , CM000671.1:g.140093867C>A GRCh37
NC_000009.10:g.139213688C>A NCBI36
NG_027801.1:g.6297G>T
NG_027801.2:g.9779G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1297G>T MANE Select ENSP00000387100.4:p.Ala433Ser
ENST00000333046.8:c.691G>T ENSP00000327617.4:p.Ala231Ser
ENST00000409012.4:c.1297G>T ENSP00000387100.4:p.Ala433Ser
ENST00000541945.1:n.90+4689G>T
NM_001128228.2:c.1297G>T NP_001121700.2:p.Ala433Ser
NM_001128228.3:c.1297G>T MANE Select NP_001121700.2:p.Ala433Ser