Canonical Allele Identifier: CA848894918

Gene: LRRC14

Linked Data

• dbSNP Id: rs1347868639
• MyVariant Identifiers: chr8:g.145744311A>G (hg19) ; chr8:g.144518927A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144518927A>G , CM000670.2:g.144518927A>G	GRCh38
NC_000008.10:g.145744311A>G , CM000670.1:g.145744311A>G	GRCh37
NC_000008.9:g.145715119A>G	NCBI36
NG_016430.1:g.3900T>C
NG_033083.1:g.5963A>G
NG_016430.2:g.3900T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292524.6:c.-111-688A>G MANE Select	ENSP00000292524.1:n.-111-688A>G
ENST00000292524.5:c.-111-688A>G	ENSP00000292524.1:n.-111-688A>G
ENST00000525766.1:c.-112+112A>G	ENSP00000434738.1:n.-112+112A>G
ENST00000527730.1:c.-25-774A>G	ENSP00000436452.1:n.-25-774A>G
ENST00000529022.5:c.-112+112A>G	ENSP00000434768.1:n.-112+112A>G
ENST00000530854.1:c.-26+112A>G	ENSP00000435985.1:n.-26+112A>G
NM_001272036.1:c.-112+112A>G	NP_001258965.1:n.-112+112A>G
NM_014665.3:c.-111-688A>G	NP_055480.1:n.-111-688A>G
XM_005272358.3:c.-25-774A>G	XP_005272415.1:n.-25-774A>G
XM_005272359.3:c.-26+112A>G	XP_005272416.1:n.-26+112A>G
XM_005272360.3:c.-10+886A>G	XP_005272417.1:n.-10+886A>G
XM_005272361.2:c.-375-774A>G	XP_005272418.1:n.-375-774A>G
XM_011517387.1:c.-553+112A>G	XP_011515689.1:n.-553+112A>G
XM_011517388.1:c.-10+112A>G	XP_011515690.1:n.-10+112A>G
XR_928369.1:n.121+112A>G
XR_928370.1:n.121+112A>G
XR_928371.1:n.121+112A>G
XM_005272358.5:c.-25-774A>G	XP_005272415.1:n.-25-774A>G
XM_005272359.5:c.-26+112A>G	XP_005272416.1:n.-26+112A>G
XM_005272360.5:c.-10+886A>G	XP_005272417.1:n.-10+886A>G
XM_017014005.2:c.-10+112A>G	XP_016869494.1:n.-10+112A>G
XM_024447336.1:c.-112+112A>G	XP_024303104.1:n.-112+112A>G
XM_024447337.1:c.-10+112A>G	XP_024303105.1:n.-10+112A>G
XM_024447338.1:c.-461-688A>G	XP_024303106.1:n.-461-688A>G
XM_024447339.1:c.-375-774A>G	XP_024303107.1:n.-375-774A>G
XM_024447340.1:c.-243+112A>G	XP_024303108.1:n.-243+112A>G
XM_024447341.1:c.-243+886A>G	XP_024303109.1:n.-243+886A>G
NM_014665.4:c.-111-688A>G MANE Select	NP_055480.1:n.-111-688A>G
NM_001272036.2:c.-112+112A>G	NP_001258965.1:n.-112+112A>G