Canonical Allele Identifier: CA5362792
Gene: TPRN HGNC NCBI

Linked Data

dbSNP Id: rs779804292
ExAC: 9:140093923 T / C
gnomAD v2: 9-140093923-T-C
gnomAD v4: 9-137199471-T-C
MyVariant Identifiers: chr9:g.140093923T>C (hg19) chr9:g.137199471T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199471T>C , CM000671.2:g.137199471T>C GRCh38
NC_000009.11:g.140093923T>C , CM000671.1:g.140093923T>C GRCh37
NC_000009.10:g.139213744T>C NCBI36
NG_027801.1:g.6241A>G
NG_027801.2:g.9723A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1241A>G MANE Select ENSP00000387100.4:p.Gln414Arg
ENST00000333046.8:c.635A>G ENSP00000327617.4:p.Gln212Arg
ENST00000409012.4:c.1241A>G ENSP00000387100.4:p.Gln414Arg
ENST00000541945.1:n.90+4633A>G
NM_001128228.2:c.1241A>G NP_001121700.2:p.Gln414Arg
NM_001128228.3:c.1241A>G MANE Select NP_001121700.2:p.Gln414Arg
Search 100 bp 5'
Search 100 bp 3'