Canonical Allele Identifier: CA1826370995

Gene: LRRC14

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144519080_144519081delinsAT , CM000670.2:g.144519080_144519081delinsAT	GRCh38
NC_000008.10:g.145744464_145744465delinsAT , CM000670.1:g.145744464_145744465delinsAT	GRCh37
NC_000008.9:g.145715272_145715273delinsAT	NCBI36
NG_016430.1:g.3746_3747delinsAT
NG_033083.1:g.6116_6117delinsAT
NG_016430.2:g.3746_3747delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000292524.6:c.-111-535_-111-534delinsAT MANE Select	ENSP00000292524.1:n.-111-535_-111-534deli...
ENST00000292524.5:c.-111-535_-111-534delinsAT	ENSP00000292524.1:n.-111-535_-111-534deli...
ENST00000525766.1:c.-112+265_-112+266delinsAT	ENSP00000434738.1:n.-112+265_-112+266deli...
ENST00000527730.1:c.-25-621_-25-620delinsAT	ENSP00000436452.1:n.-25-621_-25-620delins...
ENST00000529022.5:c.-112+265_-112+266delinsAT	ENSP00000434768.1:n.-112+265_-112+266deli...
ENST00000530854.1:c.-26+265_-26+266delinsAT	ENSP00000435985.1:n.-26+265_-26+266delins...
NM_001272036.1:c.-112+265_-112+266delinsAT	NP_001258965.1:n.-112+265_-112+266delinsA...
NM_014665.3:c.-111-535_-111-534delinsAT	NP_055480.1:n.-111-535_-111-534delinsAT
XM_005272358.3:c.-25-621_-25-620delinsAT	XP_005272415.1:n.-25-621_-25-620delinsAT
XM_005272359.3:c.-26+265_-26+266delinsAT	XP_005272416.1:n.-26+265_-26+266delinsAT
XM_005272360.3:c.-9-754_-9-753delinsAT	XP_005272417.1:n.-9-754_-9-753delinsAT
XM_005272361.2:c.-375-621_-375-620delinsAT	XP_005272418.1:n.-375-621_-375-620delinsA...
XM_011517387.1:c.-552-94_-552-93delinsAT	XP_011515689.1:n.-552-94_-552-93delinsAT
XM_011517388.1:c.-10+265_-10+266delinsAT	XP_011515690.1:n.-10+265_-10+266delinsAT
XR_928369.1:n.121+265_121+266delinsAT
XR_928370.1:n.121+265_121+266delinsAT
XR_928371.1:n.121+265_121+266delinsAT
XM_005272358.5:c.-25-621_-25-620delinsAT	XP_005272415.1:n.-25-621_-25-620delinsAT
XM_005272359.5:c.-26+265_-26+266delinsAT	XP_005272416.1:n.-26+265_-26+266delinsAT
XM_005272360.5:c.-9-754_-9-753delinsAT	XP_005272417.1:n.-9-754_-9-753delinsAT
XM_017014005.2:c.-10+265_-10+266delinsAT	XP_016869494.1:n.-10+265_-10+266delinsAT
XM_024447336.1:c.-112+265_-112+266delinsAT	XP_024303104.1:n.-112+265_-112+266delinsA...
XM_024447337.1:c.-10+265_-10+266delinsAT	XP_024303105.1:n.-10+265_-10+266delinsAT
XM_024447338.1:c.-461-535_-461-534delinsAT	XP_024303106.1:n.-461-535_-461-534delinsA...
XM_024447339.1:c.-375-621_-375-620delinsAT	XP_024303107.1:n.-375-621_-375-620delinsA...
XM_024447340.1:c.-243+265_-243+266delinsAT	XP_024303108.1:n.-243+265_-243+266delinsA...
XM_024447341.1:c.-242-754_-242-753delinsAT	XP_024303109.1:n.-242-754_-242-753delinsA...
NM_014665.4:c.-111-535_-111-534delinsAT MANE Select	NP_055480.1:n.-111-535_-111-534delinsAT
NM_001272036.2:c.-112+265_-112+266delinsAT	NP_001258965.1:n.-112+265_-112+266delinsA...