Canonical Allele Identifier: CA1826370997
Gene: LRRC14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144519083_144519088delinsTTATAG , CM000670.2:g.144519083_144519088delinsTTATAG GRCh38
NC_000008.10:g.145744467_145744472delinsTTATAG , CM000670.1:g.145744467_145744472delinsTTATAG GRCh37
NC_000008.9:g.145715275_145715280delinsTTATAG NCBI36
NG_016430.1:g.3739_3744delinsCTATAA
NG_033083.1:g.6119_6124delinsTTATAG
NG_016430.2:g.3739_3744delinsCTATAA

Transcript Alleles

HGVS Amino-acid change
ENST00000292524.6:c.-111-532_-111-527delinsTTATAG MANE Select ENSP00000292524.1:n.-111-532_-111-527deli...
ENST00000292524.5:c.-111-532_-111-527delinsTTATAG ENSP00000292524.1:n.-111-532_-111-527deli...
ENST00000525766.1:c.-112+268_-112+273delinsTTATAG ENSP00000434738.1:n.-112+268_-112+273deli...
ENST00000527730.1:c.-25-618_-25-613delinsTTATAG ENSP00000436452.1:n.-25-618_-25-613delins...
ENST00000529022.5:c.-112+268_-112+273delinsTTATAG ENSP00000434768.1:n.-112+268_-112+273deli...
ENST00000530854.1:c.-26+268_-26+273delinsTTATAG ENSP00000435985.1:n.-26+268_-26+273delins...
NM_001272036.1:c.-112+268_-112+273delinsTTATAG NP_001258965.1:n.-112+268_-112+273delinsT...
NM_014665.3:c.-111-532_-111-527delinsTTATAG NP_055480.1:n.-111-532_-111-527delinsTTAT...
XM_005272358.3:c.-25-618_-25-613delinsTTATAG XP_005272415.1:n.-25-618_-25-613delinsTTA...
XM_005272359.3:c.-26+268_-26+273delinsTTATAG XP_005272416.1:n.-26+268_-26+273delinsTTA...
XM_005272360.3:c.-9-751_-9-746delinsTTATAG XP_005272417.1:n.-9-751_-9-746delinsTTATA...
XM_005272361.2:c.-375-618_-375-613delinsTTATAG XP_005272418.1:n.-375-618_-375-613delinsT...
XM_011517387.1:c.-552-91_-552-86delinsTTATAG XP_011515689.1:n.-552-91_-552-86delinsTTA...
XM_011517388.1:c.-10+268_-10+273delinsTTATAG XP_011515690.1:n.-10+268_-10+273delinsTTA...
XR_928369.1:n.121+268_121+273delinsTTATAG
XR_928370.1:n.121+268_121+273delinsTTATAG
XR_928371.1:n.121+268_121+273delinsTTATAG
XM_005272358.5:c.-25-618_-25-613delinsTTATAG XP_005272415.1:n.-25-618_-25-613delinsTTA...
XM_005272359.5:c.-26+268_-26+273delinsTTATAG XP_005272416.1:n.-26+268_-26+273delinsTTA...
XM_005272360.5:c.-9-751_-9-746delinsTTATAG XP_005272417.1:n.-9-751_-9-746delinsTTATA...
XM_017014005.2:c.-10+268_-10+273delinsTTATAG XP_016869494.1:n.-10+268_-10+273delinsTTA...
XM_024447336.1:c.-112+268_-112+273delinsTTATAG XP_024303104.1:n.-112+268_-112+273delinsT...
XM_024447337.1:c.-10+268_-10+273delinsTTATAG XP_024303105.1:n.-10+268_-10+273delinsTTA...
XM_024447338.1:c.-461-532_-461-527delinsTTATAG XP_024303106.1:n.-461-532_-461-527delinsT...
XM_024447339.1:c.-375-618_-375-613delinsTTATAG XP_024303107.1:n.-375-618_-375-613delinsT...
XM_024447340.1:c.-243+268_-243+273delinsTTATAG XP_024303108.1:n.-243+268_-243+273delinsT...
XM_024447341.1:c.-242-751_-242-746delinsTTATAG XP_024303109.1:n.-242-751_-242-746delinsT...
NM_014665.4:c.-111-532_-111-527delinsTTATAG MANE Select NP_055480.1:n.-111-532_-111-527delinsTTAT...
NM_001272036.2:c.-112+268_-112+273delinsTTATAG NP_001258965.1:n.-112+268_-112+273delinsT...