Canonical Allele Identifier: CA375776633
Gene: TPRN HGNC NCBI

Linked Data

dbSNP Id: rs1394571612
gnomAD v2: 9-140093831-T-C
gnomAD v4: 9-137199379-T-C
MyVariant Identifiers: chr9:g.140093831T>C (hg19) chr9:g.137199379T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199379T>C , CM000671.2:g.137199379T>C GRCh38
NC_000009.11:g.140093831T>C , CM000671.1:g.140093831T>C GRCh37
NC_000009.10:g.139213652T>C NCBI36
NG_027801.1:g.6333A>G
NG_027801.2:g.9815A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000409012.6:c.1333A>G MANE Select ENSP00000387100.4:p.Ser445Gly
ENST00000333046.8:c.727A>G ENSP00000327617.4:p.Ser243Gly
ENST00000409012.4:c.1333A>G ENSP00000387100.4:p.Ser445Gly
ENST00000541945.1:n.90+4725A>G
NM_001128228.2:c.1333A>G NP_001121700.2:p.Ser445Gly
NM_001128228.3:c.1333A>G MANE Select NP_001121700.2:p.Ser445Gly
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