Canonical Allele Identifier: CA5362789
Gene: TPRN HGNC NCBI

Linked Data

dbSNP Id: rs768119327
ExAC: 9:140093910 T / A
gnomAD v2: 9-140093910-T-A
gnomAD v4: 9-137199458-T-A
MyVariant Identifiers: chr9:g.140093910T>A (hg19) chr9:g.137199458T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199458T>A , CM000671.2:g.137199458T>A GRCh38
NC_000009.11:g.140093910T>A , CM000671.1:g.140093910T>A GRCh37
NC_000009.10:g.139213731T>A NCBI36
NG_027801.1:g.6254A>T
NG_027801.2:g.9736A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1254A>T MANE Select ENSP00000387100.4:p.Ser418=
ENST00000333046.8:c.648A>T ENSP00000327617.4:p.Ser216=
ENST00000409012.4:c.1254A>T ENSP00000387100.4:p.Ser418=
ENST00000541945.1:n.90+4646A>T
NM_001128228.2:c.1254A>T NP_001121700.2:p.Ser418=
NM_001128228.3:c.1254A>T MANE Select NP_001121700.2:p.Ser418=
Search 100 bp 5'
Search 100 bp 3'