Canonical Allele Identifier: CA1826370892

Gene: LRRC14

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144518915T= , CM000670.2:g.144518915T=	GRCh38
NC_000008.10:g.145744299T= , CM000670.1:g.145744299T=	GRCh37
NC_000008.9:g.145715107T=	NCBI36
NG_016430.1:g.3912A=
NG_033083.1:g.5951T=
NG_016430.2:g.3912A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292524.6:c.-111-700T= MANE Select	ENSP00000292524.1:n.-111-700T=
ENST00000292524.5:c.-111-700T=	ENSP00000292524.1:n.-111-700T=
ENST00000525766.1:c.-112+100T=	ENSP00000434738.1:n.-112+100T=
ENST00000527730.1:c.-25-786T=	ENSP00000436452.1:n.-25-786T=
ENST00000529022.5:c.-112+100T=	ENSP00000434768.1:n.-112+100T=
ENST00000530854.1:c.-26+100T=	ENSP00000435985.1:n.-26+100T=
NM_001272036.1:c.-112+100T=	NP_001258965.1:n.-112+100T=
NM_014665.3:c.-111-700T=	NP_055480.1:n.-111-700T=
XM_005272358.3:c.-25-786T=	XP_005272415.1:n.-25-786T=
XM_005272359.3:c.-26+100T=	XP_005272416.1:n.-26+100T=
XM_005272360.3:c.-10+874T=	XP_005272417.1:n.-10+874T=
XM_005272361.2:c.-375-786T=	XP_005272418.1:n.-375-786T=
XM_011517387.1:c.-553+100T=	XP_011515689.1:n.-553+100T=
XM_011517388.1:c.-10+100T=	XP_011515690.1:n.-10+100T=
XR_928369.1:n.121+100T=
XR_928370.1:n.121+100T=
XR_928371.1:n.121+100T=
XM_005272358.5:c.-25-786T=	XP_005272415.1:n.-25-786T=
XM_005272359.5:c.-26+100T=	XP_005272416.1:n.-26+100T=
XM_005272360.5:c.-10+874T=	XP_005272417.1:n.-10+874T=
XM_017014005.2:c.-10+100T=	XP_016869494.1:n.-10+100T=
XM_024447336.1:c.-112+100T=	XP_024303104.1:n.-112+100T=
XM_024447337.1:c.-10+100T=	XP_024303105.1:n.-10+100T=
XM_024447338.1:c.-461-700T=	XP_024303106.1:n.-461-700T=
XM_024447339.1:c.-375-786T=	XP_024303107.1:n.-375-786T=
XM_024447340.1:c.-243+100T=	XP_024303108.1:n.-243+100T=
XM_024447341.1:c.-243+874T=	XP_024303109.1:n.-243+874T=
NM_014665.4:c.-111-700T= MANE Select	NP_055480.1:n.-111-700T=
NM_001272036.2:c.-112+100T=	NP_001258965.1:n.-112+100T=