Canonical Allele Identifier: CA2838196888
Gene: TRIM63 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26057748G>T , CM000663.2:g.26057748G>T GRCh38
NC_000001.10:g.26384239G>T , CM000663.1:g.26384239G>T GRCh37
NC_000001.9:g.26256826G>T NCBI36
NG_033268.1:g.14887C>A , LRG_757:g.14887C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374272.4:c.832-98C>A MANE Select ENSP00000363390.3:n.832-98C>A
ENST00000374272.3:c.832-98C>A ENSP00000363390.3:n.832-98C>A
NM_032588.3:c.832-98C>A , LRG_757t1:c.832-98C>A NP_115977.2:n.832-98C>A
XM_017002559.2:c.832-98C>A XP_016858048.1:n.832-98C>A
NM_032588.4:c.832-98C>A MANE Select NP_115977.2:n.832-98C>A
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