Canonical Allele Identifier: CA375776152
Gene: TPRN HGNC NCBI

Linked Data

gnomAD v4: 9-137199315-G-A
MyVariant Identifiers: chr9:g.140093767G>A (hg19) chr9:g.137199315G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137199315G>A , CM000671.2:g.137199315G>A GRCh38
NC_000009.11:g.140093767G>A , CM000671.1:g.140093767G>A GRCh37
NC_000009.10:g.139213588G>A NCBI36
NG_027801.1:g.6397C>T
NG_027801.2:g.9879C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409012.6:c.1397C>T MANE Select ENSP00000387100.4:p.Ala466Val
ENST00000333046.8:c.791C>T ENSP00000327617.4:p.Ala264Val
ENST00000409012.4:c.1397C>T ENSP00000387100.4:p.Ala466Val
ENST00000541945.1:n.90+4789C>T
NM_001128228.2:c.1397C>T NP_001121700.2:p.Ala466Val
NM_001128228.3:c.1397C>T MANE Select NP_001121700.2:p.Ala466Val
Search 100 bp 5'
Search 100 bp 3'