Canonical Allele Identifier: CA375769102
Gene: TPRN HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.140086737C>A (hg19) chr9:g.137192285C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137192285C>A , CM000671.2:g.137192285C>A GRCh38
NC_000009.11:g.140086737C>A , CM000671.1:g.140086737C>A GRCh37
NC_000009.10:g.139206558C>A NCBI36
NG_027801.1:g.13427G>T
NG_027801.2:g.16909G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000409012.6:c.2047G>T MANE Select ENSP00000387100.4:p.Ala683Ser
ENST00000333046.8:c.1441G>T ENSP00000327617.4:p.Ala481Ser
ENST00000409012.4:c.2047G>T ENSP00000387100.4:p.Ala683Ser
ENST00000477345.1:n.2768G>T
NM_001128228.2:c.2047G>T NP_001121700.2:p.Ala683Ser
NM_001128228.3:c.2047G>T MANE Select NP_001121700.2:p.Ala683Ser
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