Canonical Allele Identifier: CA467925002
Gene: TPRN HGNC NCBI

Linked Data

gnomAD v4: 9-137199440-C-A
MyVariant Identifiers: chr9:g.140093892C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199440C>A , CM000671.2:g.137199440C>A GRCh38
NC_000009.11:g.140093892C>A , CM000671.1:g.140093892C>A GRCh37
NC_000009.10:g.139213713C>A NCBI36
NG_027801.1:g.6272G>T
NG_027801.2:g.9754G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1272G>T MANE Select ENSP00000387100.4:p.Pro424=
ENST00000333046.8:c.666G>T ENSP00000327617.4:p.Pro222=
ENST00000409012.4:c.1272G>T ENSP00000387100.4:p.Pro424=
ENST00000541945.1:n.90+4664G>T
NM_001128228.2:c.1272G>T NP_001121700.2:p.Pro424=
NM_001128228.3:c.1272G>T MANE Select NP_001121700.2:p.Pro424=
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