Canonical Allele Identifier: CA1826370947
Gene: LRRC14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144519009A= , CM000670.2:g.144519009A= GRCh38
NC_000008.10:g.145744393A= , CM000670.1:g.145744393A= GRCh37
NC_000008.9:g.145715201A= NCBI36
NG_016430.1:g.3818T=
NG_033083.1:g.6045A=
NG_016430.2:g.3818T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000292524.6:c.-111-606A= MANE Select ENSP00000292524.1:n.-111-606A=
ENST00000292524.5:c.-111-606A= ENSP00000292524.1:n.-111-606A=
ENST00000525766.1:c.-112+194A= ENSP00000434738.1:n.-112+194A=
ENST00000527730.1:c.-25-692A= ENSP00000436452.1:n.-25-692A=
ENST00000529022.5:c.-112+194A= ENSP00000434768.1:n.-112+194A=
ENST00000530854.1:c.-26+194A= ENSP00000435985.1:n.-26+194A=
NM_001272036.1:c.-112+194A= NP_001258965.1:n.-112+194A=
NM_014665.3:c.-111-606A= NP_055480.1:n.-111-606A=
XM_005272358.3:c.-25-692A= XP_005272415.1:n.-25-692A=
XM_005272359.3:c.-26+194A= XP_005272416.1:n.-26+194A=
XM_005272360.3:c.-9-825A= XP_005272417.1:n.-9-825A=
XM_005272361.2:c.-375-692A= XP_005272418.1:n.-375-692A=
XM_011517387.1:c.-552-165A= XP_011515689.1:n.-552-165A=
XM_011517388.1:c.-10+194A= XP_011515690.1:n.-10+194A=
XR_928369.1:n.121+194A=
XR_928370.1:n.121+194A=
XR_928371.1:n.121+194A=
XM_005272358.5:c.-25-692A= XP_005272415.1:n.-25-692A=
XM_005272359.5:c.-26+194A= XP_005272416.1:n.-26+194A=
XM_005272360.5:c.-9-825A= XP_005272417.1:n.-9-825A=
XM_017014005.2:c.-10+194A= XP_016869494.1:n.-10+194A=
XM_024447336.1:c.-112+194A= XP_024303104.1:n.-112+194A=
XM_024447337.1:c.-10+194A= XP_024303105.1:n.-10+194A=
XM_024447338.1:c.-461-606A= XP_024303106.1:n.-461-606A=
XM_024447339.1:c.-375-692A= XP_024303107.1:n.-375-692A=
XM_024447340.1:c.-243+194A= XP_024303108.1:n.-243+194A=
XM_024447341.1:c.-242-825A= XP_024303109.1:n.-242-825A=
NM_014665.4:c.-111-606A= MANE Select NP_055480.1:n.-111-606A=
NM_001272036.2:c.-112+194A= NP_001258965.1:n.-112+194A=