Canonical Allele Identifier: CA1826370906

Gene: LRRC14

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144518939_144518940delinsTG , CM000670.2:g.144518939_144518940delinsTG	GRCh38
NC_000008.10:g.145744323_145744324delinsTG , CM000670.1:g.145744323_145744324delinsTG	GRCh37
NC_000008.9:g.145715131_145715132delinsTG	NCBI36
NG_016430.1:g.3887_3888delinsCA
NG_033083.1:g.5975_5976delinsTG
NG_016430.2:g.3887_3888delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292524.6:c.-111-676_-111-675delinsTG MANE Select	ENSP00000292524.1:n.-111-676_-111-675delinsTG
ENST00000292524.5:c.-111-676_-111-675delinsTG	ENSP00000292524.1:n.-111-676_-111-675delinsTG
ENST00000525766.1:c.-112+124_-112+125delinsTG	ENSP00000434738.1:n.-112+124_-112+125delinsTG
ENST00000527730.1:c.-25-762_-25-761delinsTG	ENSP00000436452.1:n.-25-762_-25-761delinsTG
ENST00000529022.5:c.-112+124_-112+125delinsTG	ENSP00000434768.1:n.-112+124_-112+125delinsTG
ENST00000530854.1:c.-26+124_-26+125delinsTG	ENSP00000435985.1:n.-26+124_-26+125delinsTG
NM_001272036.1:c.-112+124_-112+125delinsTG	NP_001258965.1:n.-112+124_-112+125delinsTG
NM_014665.3:c.-111-676_-111-675delinsTG	NP_055480.1:n.-111-676_-111-675delinsTG
XM_005272358.3:c.-25-762_-25-761delinsTG	XP_005272415.1:n.-25-762_-25-761delinsTG
XM_005272359.3:c.-26+124_-26+125delinsTG	XP_005272416.1:n.-26+124_-26+125delinsTG
XM_005272360.3:c.-9-895_-9-894delinsTG	XP_005272417.1:n.-9-895_-9-894delinsTG
XM_005272361.2:c.-375-762_-375-761delinsTG	XP_005272418.1:n.-375-762_-375-761delinsTG
XM_011517387.1:c.-553+124_-553+125delinsTG	XP_011515689.1:n.-553+124_-553+125delinsTG
XM_011517388.1:c.-10+124_-10+125delinsTG	XP_011515690.1:n.-10+124_-10+125delinsTG
XR_928369.1:n.121+124_121+125delinsTG
XR_928370.1:n.121+124_121+125delinsTG
XR_928371.1:n.121+124_121+125delinsTG
XM_005272358.5:c.-25-762_-25-761delinsTG	XP_005272415.1:n.-25-762_-25-761delinsTG
XM_005272359.5:c.-26+124_-26+125delinsTG	XP_005272416.1:n.-26+124_-26+125delinsTG
XM_005272360.5:c.-9-895_-9-894delinsTG	XP_005272417.1:n.-9-895_-9-894delinsTG
XM_017014005.2:c.-10+124_-10+125delinsTG	XP_016869494.1:n.-10+124_-10+125delinsTG
XM_024447336.1:c.-112+124_-112+125delinsTG	XP_024303104.1:n.-112+124_-112+125delinsTG
XM_024447337.1:c.-10+124_-10+125delinsTG	XP_024303105.1:n.-10+124_-10+125delinsTG
XM_024447338.1:c.-461-676_-461-675delinsTG	XP_024303106.1:n.-461-676_-461-675delinsTG
XM_024447339.1:c.-375-762_-375-761delinsTG	XP_024303107.1:n.-375-762_-375-761delinsTG
XM_024447340.1:c.-243+124_-243+125delinsTG	XP_024303108.1:n.-243+124_-243+125delinsTG
XM_024447341.1:c.-242-895_-242-894delinsTG	XP_024303109.1:n.-242-895_-242-894delinsTG
NM_014665.4:c.-111-676_-111-675delinsTG MANE Select	NP_055480.1:n.-111-676_-111-675delinsTG
NM_001272036.2:c.-112+124_-112+125delinsTG	NP_001258965.1:n.-112+124_-112+125delinsTG