Canonical Allele Identifier: CA375777188
Gene: TPRN HGNC NCBI

Linked Data

gnomAD v4: 9-137199489-T-C
MyVariant Identifiers: chr9:g.140093941T>C (hg19) chr9:g.137199489T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199489T>C , CM000671.2:g.137199489T>C GRCh38
NC_000009.11:g.140093941T>C , CM000671.1:g.140093941T>C GRCh37
NC_000009.10:g.139213762T>C NCBI36
NG_027801.1:g.6223A>G
NG_027801.2:g.9705A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000409012.6:c.1223A>G MANE Select ENSP00000387100.4:p.Asp408Gly
ENST00000333046.8:c.617A>G ENSP00000327617.4:p.Asp206Gly
ENST00000409012.4:c.1223A>G ENSP00000387100.4:p.Asp408Gly
ENST00000541945.1:n.90+4615A>G
NM_001128228.2:c.1223A>G NP_001121700.2:p.Asp408Gly
NM_001128228.3:c.1223A>G MANE Select NP_001121700.2:p.Asp408Gly
Search 100 bp 5'
Search 100 bp 3'