Canonical Allele Identifier: CA375775899
Gene: TPRN HGNC NCBI

Linked Data

gnomAD v4: 9-137199282-T-C
MyVariant Identifiers: chr9:g.140093734T>C (hg19) chr9:g.137199282T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199282T>C , CM000671.2:g.137199282T>C GRCh38
NC_000009.11:g.140093734T>C , CM000671.1:g.140093734T>C GRCh37
NC_000009.10:g.139213555T>C NCBI36
NG_027801.1:g.6430A>G
NG_027801.2:g.9912A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1430A>G MANE Select ENSP00000387100.4:p.His477Arg
ENST00000333046.8:c.824A>G ENSP00000327617.4:p.His275Arg
ENST00000409012.4:c.1430A>G ENSP00000387100.4:p.His477Arg
ENST00000541945.1:n.90+4822A>G
NM_001128228.2:c.1430A>G NP_001121700.2:p.His477Arg
NM_001128228.3:c.1430A>G MANE Select NP_001121700.2:p.His477Arg
Search 100 bp 5'
Search 100 bp 3'