Canonical Allele Identifier: CA12850463
Gene: LRRC14 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2721173

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144519045C>T , CM000670.2:g.144519045C>T GRCh38
NC_000008.10:g.145744429C>T , CM000670.1:g.145744429C>T GRCh37
NC_000008.9:g.145715237C>T NCBI36
NG_016430.1:g.3782G>A
NG_033083.1:g.6081C>T

Transcript Alleles

HGVS Amino-acid change
NM_001272036.1:c.-112+230C>T VV NP_001258965.1:p.=
NM_014665.3:c.-111-570C>T VV NP_055480.1:p.=
XM_005272358.3:c.-25-656C>T XP_005272415.1:p.=
XM_005272359.3:c.-26+230C>T XP_005272416.1:p.=
XM_005272360.3:c.-9-789C>T XP_005272417.1:p.=
XM_005272361.2:c.-375-656C>T XP_005272418.1:p.=
XM_011517387.1:c.-552-129C>T XP_011515689.1:p.=
XM_011517388.1:c.-10+230C>T XP_011515690.1:p.=
XR_928369.1:n.121+230C>T
XR_928370.1:n.121+230C>T
XR_928371.1:n.121+230C>T
XM_005272358.5:c.-25-656C>T XP_005272415.1:p.=
XM_005272359.5:c.-26+230C>T XP_005272416.1:p.=
XM_005272360.5:c.-9-789C>T XP_005272417.1:p.=
XM_017014005.2:c.-10+230C>T XP_016869494.1:p.=
XM_024447336.1:c.-112+230C>T XP_024303104.1:p.=
XM_024447337.1:c.-10+230C>T XP_024303105.1:p.=
XM_024447338.1:c.-461-570C>T XP_024303106.1:p.=
XM_024447339.1:c.-375-656C>T XP_024303107.1:p.=
XM_024447340.1:c.-243+230C>T XP_024303108.1:p.=
XM_024447341.1:c.-242-789C>T XP_024303109.1:p.=
NM_014665.4:c.-111-570C>T VV MANE Preferred NP_055480.1:p.=
ENST00000292524.5:c.-111-570C>T ENSP00000292524.1:p.=
ENST00000525766.1:c.-112+230C>T ENSP00000434738.1:p.=
ENST00000527730.1:c.-25-656C>T ENSP00000436452.1:p.=
ENST00000529022.5:c.-112+230C>T ENSP00000434768.1:p.=
ENST00000530854.1:c.-26+230C>T ENSP00000435985.1:p.=