Canonical Allele Identifier: CA1826370946
Gene: LRRC14 HGNC NCBI

Linked Data

dbSNP Id: rs1815723166

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144519008G>A , CM000670.2:g.144519008G>A GRCh38
NC_000008.10:g.145744392G>A , CM000670.1:g.145744392G>A GRCh37
NC_000008.9:g.145715200G>A NCBI36
NG_016430.1:g.3819C>T
NG_033083.1:g.6044G>A
NG_016430.2:g.3819C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000292524.6:c.-111-607G>A MANE Select ENSP00000292524.1:n.-111-607G>A
ENST00000292524.5:c.-111-607G>A ENSP00000292524.1:n.-111-607G>A
ENST00000525766.1:c.-112+193G>A ENSP00000434738.1:n.-112+193G>A
ENST00000527730.1:c.-25-693G>A ENSP00000436452.1:n.-25-693G>A
ENST00000529022.5:c.-112+193G>A ENSP00000434768.1:n.-112+193G>A
ENST00000530854.1:c.-26+193G>A ENSP00000435985.1:n.-26+193G>A
NM_001272036.1:c.-112+193G>A NP_001258965.1:n.-112+193G>A
NM_014665.3:c.-111-607G>A NP_055480.1:n.-111-607G>A
XM_005272358.3:c.-25-693G>A XP_005272415.1:n.-25-693G>A
XM_005272359.3:c.-26+193G>A XP_005272416.1:n.-26+193G>A
XM_005272360.3:c.-9-826G>A XP_005272417.1:n.-9-826G>A
XM_005272361.2:c.-375-693G>A XP_005272418.1:n.-375-693G>A
XM_011517387.1:c.-552-166G>A XP_011515689.1:n.-552-166G>A
XM_011517388.1:c.-10+193G>A XP_011515690.1:n.-10+193G>A
XR_928369.1:n.121+193G>A
XR_928370.1:n.121+193G>A
XR_928371.1:n.121+193G>A
XM_005272358.5:c.-25-693G>A XP_005272415.1:n.-25-693G>A
XM_005272359.5:c.-26+193G>A XP_005272416.1:n.-26+193G>A
XM_005272360.5:c.-9-826G>A XP_005272417.1:n.-9-826G>A
XM_017014005.2:c.-10+193G>A XP_016869494.1:n.-10+193G>A
XM_024447336.1:c.-112+193G>A XP_024303104.1:n.-112+193G>A
XM_024447337.1:c.-10+193G>A XP_024303105.1:n.-10+193G>A
XM_024447338.1:c.-461-607G>A XP_024303106.1:n.-461-607G>A
XM_024447339.1:c.-375-693G>A XP_024303107.1:n.-375-693G>A
XM_024447340.1:c.-243+193G>A XP_024303108.1:n.-243+193G>A
XM_024447341.1:c.-242-826G>A XP_024303109.1:n.-242-826G>A
NM_014665.4:c.-111-607G>A MANE Select NP_055480.1:n.-111-607G>A
NM_001272036.2:c.-112+193G>A NP_001258965.1:n.-112+193G>A