Canonical Allele Identifier: CA375777392
Gene: TPRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199549A>C , CM000671.2:g.137199549A>C GRCh38
NC_000009.11:g.140094001A>C , CM000671.1:g.140094001A>C GRCh37
NC_000009.10:g.139213822A>C NCBI36
NG_027801.1:g.6163T>G
NG_027801.2:g.9645T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1163T>G MANE Select ENSP00000387100.4:p.Val388Gly
ENST00000333046.8:c.557T>G ENSP00000327617.4:p.Val186Gly
ENST00000409012.4:c.1163T>G ENSP00000387100.4:p.Val388Gly
ENST00000541945.1:n.90+4555T>G
NM_001128228.2:c.1163T>G NP_001121700.2:p.Val388Gly
NM_001128228.3:c.1163T>G MANE Select NP_001121700.2:p.Val388Gly