Canonical Allele Identifier: CA848895010

Gene: LRRC14

Linked Data

• dbSNP Id: rs1335687806
• MyVariant Identifiers: chr8:g.145744457G>A (hg19) ; chr8:g.144519073G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144519073G>A , CM000670.2:g.144519073G>A	GRCh38
NC_000008.10:g.145744457G>A , CM000670.1:g.145744457G>A	GRCh37
NC_000008.9:g.145715265G>A	NCBI36
NG_016430.1:g.3754C>T
NG_033083.1:g.6109G>A
NG_016430.2:g.3754C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000292524.6:c.-111-542G>A MANE Select	ENSP00000292524.1:n.-111-542G>A
ENST00000292524.5:c.-111-542G>A	ENSP00000292524.1:n.-111-542G>A
ENST00000525766.1:c.-112+258G>A	ENSP00000434738.1:n.-112+258G>A
ENST00000527730.1:c.-25-628G>A	ENSP00000436452.1:n.-25-628G>A
ENST00000529022.5:c.-112+258G>A	ENSP00000434768.1:n.-112+258G>A
ENST00000530854.1:c.-26+258G>A	ENSP00000435985.1:n.-26+258G>A
NM_001272036.1:c.-112+258G>A	NP_001258965.1:n.-112+258G>A
NM_014665.3:c.-111-542G>A	NP_055480.1:n.-111-542G>A
XM_005272358.3:c.-25-628G>A	XP_005272415.1:n.-25-628G>A
XM_005272359.3:c.-26+258G>A	XP_005272416.1:n.-26+258G>A
XM_005272360.3:c.-9-761G>A	XP_005272417.1:n.-9-761G>A
XM_005272361.2:c.-375-628G>A	XP_005272418.1:n.-375-628G>A
XM_011517387.1:c.-552-101G>A	XP_011515689.1:n.-552-101G>A
XM_011517388.1:c.-10+258G>A	XP_011515690.1:n.-10+258G>A
XR_928369.1:n.121+258G>A
XR_928370.1:n.121+258G>A
XR_928371.1:n.121+258G>A
XM_005272358.5:c.-25-628G>A	XP_005272415.1:n.-25-628G>A
XM_005272359.5:c.-26+258G>A	XP_005272416.1:n.-26+258G>A
XM_005272360.5:c.-9-761G>A	XP_005272417.1:n.-9-761G>A
XM_017014005.2:c.-10+258G>A	XP_016869494.1:n.-10+258G>A
XM_024447336.1:c.-112+258G>A	XP_024303104.1:n.-112+258G>A
XM_024447337.1:c.-10+258G>A	XP_024303105.1:n.-10+258G>A
XM_024447338.1:c.-461-542G>A	XP_024303106.1:n.-461-542G>A
XM_024447339.1:c.-375-628G>A	XP_024303107.1:n.-375-628G>A
XM_024447340.1:c.-243+258G>A	XP_024303108.1:n.-243+258G>A
XM_024447341.1:c.-242-761G>A	XP_024303109.1:n.-242-761G>A
NM_014665.4:c.-111-542G>A MANE Select	NP_055480.1:n.-111-542G>A
NM_001272036.2:c.-112+258G>A	NP_001258965.1:n.-112+258G>A