Canonical Allele Identifier: CA1826370996
Gene: LRRC14 HGNC NCBI

Linked Data

dbSNP Id: rs1815739198

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144519084del , CM000670.2:g.144519084del GRCh38
NC_000008.10:g.145744468del , CM000670.1:g.145744468del GRCh37
NC_000008.9:g.145715276del NCBI36
NG_016430.1:g.3746del
NG_033083.1:g.6120del
NG_016430.2:g.3746del

Transcript Alleles

HGVS Amino-acid change
ENST00000292524.6:c.-111-531del MANE Select ENSP00000292524.1:n.-111-531del
ENST00000292524.5:c.-111-531del ENSP00000292524.1:n.-111-531del
ENST00000525766.1:c.-112+269del ENSP00000434738.1:n.-112+269del
ENST00000527730.1:c.-25-617del ENSP00000436452.1:n.-25-617del
ENST00000529022.5:c.-112+269del ENSP00000434768.1:n.-112+269del
ENST00000530854.1:c.-26+269del ENSP00000435985.1:n.-26+269del
NM_001272036.1:c.-112+269del NP_001258965.1:n.-112+269del
NM_014665.3:c.-111-531del NP_055480.1:n.-111-531del
XM_005272358.3:c.-25-617del XP_005272415.1:n.-25-617del
XM_005272359.3:c.-26+269del XP_005272416.1:n.-26+269del
XM_005272360.3:c.-9-750del XP_005272417.1:n.-9-750del
XM_005272361.2:c.-375-617del XP_005272418.1:n.-375-617del
XM_011517387.1:c.-552-90del XP_011515689.1:n.-552-90del
XM_011517388.1:c.-10+269del XP_011515690.1:n.-10+269del
XR_928369.1:n.121+269del
XR_928370.1:n.121+269del
XR_928371.1:n.121+269del
XM_005272358.5:c.-25-617del XP_005272415.1:n.-25-617del
XM_005272359.5:c.-26+269del XP_005272416.1:n.-26+269del
XM_005272360.5:c.-9-750del XP_005272417.1:n.-9-750del
XM_017014005.2:c.-10+269del XP_016869494.1:n.-10+269del
XM_024447336.1:c.-112+269del XP_024303104.1:n.-112+269del
XM_024447337.1:c.-10+269del XP_024303105.1:n.-10+269del
XM_024447338.1:c.-461-531del XP_024303106.1:n.-461-531del
XM_024447339.1:c.-375-617del XP_024303107.1:n.-375-617del
XM_024447340.1:c.-243+269del XP_024303108.1:n.-243+269del
XM_024447341.1:c.-242-750del XP_024303109.1:n.-242-750del
NM_014665.4:c.-111-531del MANE Select NP_055480.1:n.-111-531del
NM_001272036.2:c.-112+269del NP_001258965.1:n.-112+269del