Canonical Allele Identifier: CA187693541
Gene: LRRC14 HGNC NCBI

Linked Data

dbSNP Id: rs1034567342

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144519090C>T , CM000670.2:g.144519090C>T GRCh38
NC_000008.10:g.145744474C>T , CM000670.1:g.145744474C>T GRCh37
NC_000008.9:g.145715282C>T NCBI36
NG_016430.1:g.3737G>A
NG_033083.1:g.6126C>T
NG_016430.2:g.3737G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000292524.6:c.-111-525C>T MANE Select ENSP00000292524.1:n.-111-525C>T
ENST00000292524.5:c.-111-525C>T ENSP00000292524.1:n.-111-525C>T
ENST00000525766.1:c.-112+275C>T ENSP00000434738.1:n.-112+275C>T
ENST00000527730.1:c.-25-611C>T ENSP00000436452.1:n.-25-611C>T
ENST00000529022.5:c.-112+275C>T ENSP00000434768.1:n.-112+275C>T
ENST00000530854.1:c.-26+275C>T ENSP00000435985.1:n.-26+275C>T
NM_001272036.1:c.-112+275C>T NP_001258965.1:n.-112+275C>T
NM_014665.3:c.-111-525C>T NP_055480.1:n.-111-525C>T
XM_005272358.3:c.-25-611C>T XP_005272415.1:n.-25-611C>T
XM_005272359.3:c.-26+275C>T XP_005272416.1:n.-26+275C>T
XM_005272360.3:c.-9-744C>T XP_005272417.1:n.-9-744C>T
XM_005272361.2:c.-375-611C>T XP_005272418.1:n.-375-611C>T
XM_011517387.1:c.-552-84C>T XP_011515689.1:n.-552-84C>T
XM_011517388.1:c.-10+275C>T XP_011515690.1:n.-10+275C>T
XR_928369.1:n.121+275C>T
XR_928370.1:n.121+275C>T
XR_928371.1:n.121+275C>T
XM_005272358.5:c.-25-611C>T XP_005272415.1:n.-25-611C>T
XM_005272359.5:c.-26+275C>T XP_005272416.1:n.-26+275C>T
XM_005272360.5:c.-9-744C>T XP_005272417.1:n.-9-744C>T
XM_017014005.2:c.-10+275C>T XP_016869494.1:n.-10+275C>T
XM_024447336.1:c.-112+275C>T XP_024303104.1:n.-112+275C>T
XM_024447337.1:c.-10+275C>T XP_024303105.1:n.-10+275C>T
XM_024447338.1:c.-461-525C>T XP_024303106.1:n.-461-525C>T
XM_024447339.1:c.-375-611C>T XP_024303107.1:n.-375-611C>T
XM_024447340.1:c.-243+275C>T XP_024303108.1:n.-243+275C>T
XM_024447341.1:c.-242-744C>T XP_024303109.1:n.-242-744C>T
NM_014665.4:c.-111-525C>T MANE Select NP_055480.1:n.-111-525C>T
NM_001272036.2:c.-112+275C>T NP_001258965.1:n.-112+275C>T