Canonical Allele Identifier: CA15862574
Gene: TRIP4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64433291T>C , CM000677.2:g.64433291T>C GRCh38
NC_000015.9:g.64725490T>C , CM000677.1:g.64725490T>C GRCh37
NC_000015.8:g.62512543T>C NCBI36
NG_046848.1:g.50488T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261884.8:c.1575+7660T>C MANE Select ENSP00000261884.3:n.1575+7660T>C
ENST00000261884.7:c.1575+7660T>C ENSP00000261884.3:n.1575+7660T>C
ENST00000558162.1:c.133+7660T>C
ENST00000560475.1:c.112-11715T>C
NM_016213.4:c.1575+7660T>C NP_057297.2:n.1575+7660T>C
XM_005254789.1:c.885+7660T>C XP_005254846.1:n.885+7660T>C
XR_243130.1:n.1506+7660T>C
NM_001321924.1:c.885+7660T>C NP_001308853.1:n.885+7660T>C
NR_135855.1:n.1508+7660T>C
NM_001321924.2:c.885+7660T>C NP_001308853.1:n.885+7660T>C
NM_016213.5:c.1575+7660T>C MANE Select NP_057297.2:n.1575+7660T>C
NR_135855.2:n.1476+7660T>C
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