Canonical Allele Identifier: CA375776092
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140093760T>A (hg19) chr9:g.137199308T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199308T>A , CM000671.2:g.137199308T>A GRCh38
NC_000009.11:g.140093760T>A , CM000671.1:g.140093760T>A GRCh37
NC_000009.10:g.139213581T>A NCBI36
NG_027801.1:g.6404A>T
NG_027801.2:g.9886A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1404A>T MANE Select ENSP00000387100.4:p.Gln468His
ENST00000333046.8:c.798A>T ENSP00000327617.4:p.Gln266His
ENST00000409012.4:c.1404A>T ENSP00000387100.4:p.Gln468His
ENST00000541945.1:n.90+4796A>T
NM_001128228.2:c.1404A>T NP_001121700.2:p.Gln468His
NM_001128228.3:c.1404A>T MANE Select NP_001121700.2:p.Gln468His
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