Canonical Allele Identifier: CA7609743
Gene: TRIP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.64445134G>A , CM000677.2:g.64445134G>A GRCh38
NC_000015.9:g.64737333G>A , CM000677.1:g.64737333G>A GRCh37
NC_000015.8:g.62524386G>A NCBI36
NG_046848.1:g.62331G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261884.8:c.1678+26G>A MANE Select ENSP00000261884.3:n.1678+26G>A
ENST00000261884.7:c.1678+26G>A ENSP00000261884.3:n.1678+26G>A
ENST00000558162.1:c.236+26G>A
ENST00000559777.1:n.185+26G>A
ENST00000560475.1:c.214+26G>A
NM_016213.4:c.1678+26G>A NP_057297.2:n.1678+26G>A
XM_005254789.1:c.988+26G>A XP_005254846.1:n.988+26G>A
XR_243130.1:n.1609+26G>A
XR_932366.1:n.350-248C>T
XR_932367.1:n.136-248C>T
NM_001321924.1:c.988+26G>A NP_001308853.1:n.988+26G>A
NR_135855.1:n.1611+26G>A
XR_932367.2:n.241-248C>T
NM_001321924.2:c.988+26G>A NP_001308853.1:n.988+26G>A
NM_016213.5:c.1678+26G>A MANE Select NP_057297.2:n.1678+26G>A
NR_135855.2:n.1579+26G>A