Canonical Allele Identifier: CA375769028
Gene: TPRN HGNC NCBI

Linked Data

gnomAD v4: 9-137192276-G-A
MyVariant Identifiers: chr9:g.140086728G>A (hg19) chr9:g.137192276G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137192276G>A , CM000671.2:g.137192276G>A GRCh38
NC_000009.11:g.140086728G>A , CM000671.1:g.140086728G>A GRCh37
NC_000009.10:g.139206549G>A NCBI36
NG_027801.1:g.13436C>T
NG_027801.2:g.16918C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000409012.6:c.2056C>T MANE Select ENSP00000387100.4:p.Pro686Ser
ENST00000333046.8:c.1450C>T ENSP00000327617.4:p.Pro484Ser
ENST00000409012.4:c.2056C>T ENSP00000387100.4:p.Pro686Ser
ENST00000477345.1:n.2777C>T
NM_001128228.2:c.2056C>T NP_001121700.2:p.Pro686Ser
NM_001128228.3:c.2056C>T MANE Select NP_001121700.2:p.Pro686Ser
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