Canonical Allele Identifier: CA271428316
Community Standard Title: NM_016213.5(TRIP4):c.1576-180G>C
Gene: TRIP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64444826G>C , CM000677.2:g.64444826G>C GRCh38
NC_000015.9:g.64737025G>C , CM000677.1:g.64737025G>C GRCh37
NC_000015.8:g.62524078G>C NCBI36
NG_046848.1:g.62023G>C

Transcript Alleles

HGVS Amino-acid Change
NM_016213.5:c.1576-180G>C MANE Select NP_057297.2:n.1576-180G>C
ENST00000261884.8:c.1576-180G>C MANE Select ENSP00000261884.3:n.1576-180G>C
NM_001321924.1:c.886-180G>C NP_001308853.1:n.886-180G>C
NM_001321924.2:c.886-180G>C NP_001308853.1:n.886-180G>C
NM_016213.4:c.1576-180G>C NP_057297.2:n.1576-180G>C
NR_135855.1:n.1509-180G>C
NR_135855.2:n.1477-180G>C
ENST00000261884.7:c.1576-180G>C ENSP00000261884.3:n.1576-180G>C
ENST00000558162.1:c.134-180G>C
ENST00000559777.1:n.82+86G>C
ENST00000560475.1:c.112-180G>C
XM_005254789.1:c.886-180G>C XP_005254846.1:n.886-180G>C
XR_243130.1:n.1507-180G>C
XR_932366.1:n.410C>G
XR_932367.1:n.196C>G
XR_932367.2:n.301C>G