Canonical Allele Identifier: CA375777149
Gene: TPRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199478T>C , CM000671.2:g.137199478T>C GRCh38
NC_000009.11:g.140093930T>C , CM000671.1:g.140093930T>C GRCh37
NC_000009.10:g.139213751T>C NCBI36
NG_027801.1:g.6234A>G
NG_027801.2:g.9716A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1234A>G MANE Select ENSP00000387100.4:p.Arg412Gly
ENST00000333046.8:c.628A>G ENSP00000327617.4:p.Arg210Gly
ENST00000409012.4:c.1234A>G ENSP00000387100.4:p.Arg412Gly
ENST00000541945.1:n.90+4626A>G
NM_001128228.2:c.1234A>G NP_001121700.2:p.Arg412Gly
NM_001128228.3:c.1234A>G MANE Select NP_001121700.2:p.Arg412Gly