Canonical Allele Identifier: CA375775790
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140093723G>A (hg19) chr9:g.137199271G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199271G>A , CM000671.2:g.137199271G>A GRCh38
NC_000009.11:g.140093723G>A , CM000671.1:g.140093723G>A GRCh37
NC_000009.10:g.139213544G>A NCBI36
NG_027801.1:g.6441C>T
NG_027801.2:g.9923C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1441C>T MANE Select ENSP00000387100.4:p.Pro481Ser
ENST00000333046.8:c.835C>T ENSP00000327617.4:p.Pro279Ser
ENST00000409012.4:c.1441C>T ENSP00000387100.4:p.Pro481Ser
ENST00000541945.1:n.90+4833C>T
NM_001128228.2:c.1441C>T NP_001121700.2:p.Pro481Ser
NM_001128228.3:c.1441C>T MANE Select NP_001121700.2:p.Pro481Ser
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