Canonical Allele Identifier: CA375777154
Gene: TPRN HGNC NCBI

Linked Data

dbSNP Id: rs1834761440
MyVariant Identifiers: chr9:g.140093931A>C (hg19) chr9:g.137199479A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199479A>C , CM000671.2:g.137199479A>C GRCh38
NC_000009.11:g.140093931A>C , CM000671.1:g.140093931A>C GRCh37
NC_000009.10:g.139213752A>C NCBI36
NG_027801.1:g.6233T>G
NG_027801.2:g.9715T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1233T>G MANE Select ENSP00000387100.4:p.Ile411Met
ENST00000333046.8:c.627T>G ENSP00000327617.4:p.Ile209Met
ENST00000409012.4:c.1233T>G ENSP00000387100.4:p.Ile411Met
ENST00000541945.1:n.90+4625T>G
NM_001128228.2:c.1233T>G NP_001121700.2:p.Ile411Met
NM_001128228.3:c.1233T>G MANE Select NP_001121700.2:p.Ile411Met
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