Canonical Allele Identifier: CA7609710
Community Standard Title: NM_016213.5(TRIP4):c.1575+35G>A
Gene: TRIP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64425666G>A , CM000677.2:g.64425666G>A GRCh38
NC_000015.9:g.64717865G>A , CM000677.1:g.64717865G>A GRCh37
NC_000015.8:g.62504918G>A NCBI36
NG_046848.1:g.42863G>A

Transcript Alleles

HGVS Amino-acid Change
NM_016213.5:c.1575+35G>A MANE Select NP_057297.2:n.1575+35G>A
ENST00000261884.8:c.1575+35G>A MANE Select ENSP00000261884.3:n.1575+35G>A
NM_001321924.1:c.885+35G>A NP_001308853.1:n.885+35G>A
NM_001321924.2:c.885+35G>A NP_001308853.1:n.885+35G>A
NM_016213.4:c.1575+35G>A NP_057297.2:n.1575+35G>A
NR_135855.1:n.1508+35G>A
NR_135855.2:n.1476+35G>A
ENST00000261884.7:c.1575+35G>A ENSP00000261884.3:n.1575+35G>A
ENST00000558162.1:c.133+35G>A
ENST00000560475.1:c.111+15838G>A
XM_005254789.1:c.885+35G>A XP_005254846.1:n.885+35G>A
XR_243130.1:n.1506+35G>A