Canonical Allele Identifier: CA467853151
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140093754G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199302G>C , CM000671.2:g.137199302G>C GRCh38
NC_000009.11:g.140093754G>C , CM000671.1:g.140093754G>C GRCh37
NC_000009.10:g.139213575G>C NCBI36
NG_027801.1:g.6410C>G
NG_027801.2:g.9892C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1410C>G MANE Select ENSP00000387100.4:p.Ala470=
ENST00000333046.8:c.804C>G ENSP00000327617.4:p.Ala268=
ENST00000409012.4:c.1410C>G ENSP00000387100.4:p.Ala470=
ENST00000541945.1:n.90+4802C>G
NM_001128228.2:c.1410C>G NP_001121700.2:p.Ala470=
NM_001128228.3:c.1410C>G MANE Select NP_001121700.2:p.Ala470=