Canonical Allele Identifier: CA375775904
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140093735G>A (hg19) chr9:g.137199283G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199283G>A , CM000671.2:g.137199283G>A GRCh38
NC_000009.11:g.140093735G>A , CM000671.1:g.140093735G>A GRCh37
NC_000009.10:g.139213556G>A NCBI36
NG_027801.1:g.6429C>T
NG_027801.2:g.9911C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1429C>T MANE Select ENSP00000387100.4:p.His477Tyr
ENST00000333046.8:c.823C>T ENSP00000327617.4:p.His275Tyr
ENST00000409012.4:c.1429C>T ENSP00000387100.4:p.His477Tyr
ENST00000541945.1:n.90+4821C>T
NM_001128228.2:c.1429C>T NP_001121700.2:p.His477Tyr
NM_001128228.3:c.1429C>T MANE Select NP_001121700.2:p.His477Tyr
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