Canonical Allele Identifier: CA375777105
Gene: TPRN HGNC NCBI

Linked Data

dbSNP Id: rs1834761194
MyVariant Identifiers: chr9:g.140093918G>T (hg19) chr9:g.137199466G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199466G>T , CM000671.2:g.137199466G>T GRCh38
NC_000009.11:g.140093918G>T , CM000671.1:g.140093918G>T GRCh37
NC_000009.10:g.139213739G>T NCBI36
NG_027801.1:g.6246C>A
NG_027801.2:g.9728C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1246C>A MANE Select ENSP00000387100.4:p.Pro416Thr
ENST00000333046.8:c.640C>A ENSP00000327617.4:p.Pro214Thr
ENST00000409012.4:c.1246C>A ENSP00000387100.4:p.Pro416Thr
ENST00000541945.1:n.90+4638C>A
NM_001128228.2:c.1246C>A NP_001121700.2:p.Pro416Thr
NM_001128228.3:c.1246C>A MANE Select NP_001121700.2:p.Pro416Thr
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