Canonical Allele Identifier: CA1966472963

Gene: LRRC4C

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.41204404T>C , CM000673.2:g.41204404T>C	GRCh38
NC_000011.9:g.41225954T>C , CM000673.1:g.41225954T>C	GRCh37
NC_000011.8:g.41182530T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528697.6:c.-496+255027A>G MANE Select	ENSP00000437132.1:n.-496+255027A>G
ENST00000528697.5:c.-496+255027A>G	ENSP00000437132.1:n.-496+255027A>G
ENST00000530763.5:c.-327+255027A>G	ENSP00000434761.1:n.-327+255027A>G
ENST00000534577.1:n.418+18393A>G
NM_001258419.1:c.-496+255027A>G	NP_001245348.1:n.-496+255027A>G
NM_020929.2:c.-327+255027A>G	NP_065980.1:n.-327+255027A>G
XM_011520238.1:c.-496+18393A>G	XP_011518540.1:n.-496+18393A>G
XM_011520239.1:c.-562+18393A>G	XP_011518541.1:n.-562+18393A>G
XM_011520240.1:c.-416+18393A>G	XP_011518542.1:n.-416+18393A>G
XM_011520243.1:c.-443+18393A>G	XP_011518545.1:n.-443+18393A>G
XM_011520244.1:c.-363+18393A>G	XP_011518546.1:n.-363+18393A>G
XM_011520238.3:c.-496+18393A>G	XP_011518540.1:n.-496+18393A>G
XM_011520239.3:c.-562+18393A>G	XP_011518541.1:n.-562+18393A>G
XM_011520240.3:c.-416+18393A>G	XP_011518542.1:n.-416+18393A>G
XM_011520243.3:c.-443+18393A>G	XP_011518545.1:n.-443+18393A>G
XM_011520244.3:c.-363+18393A>G	XP_011518546.1:n.-363+18393A>G
XM_017018070.2:c.-492+18393A>G	XP_016873559.1:n.-492+18393A>G
XM_017018071.2:c.-482+18393A>G	XP_016873560.1:n.-482+18393A>G
XM_017018072.2:c.-557+255027A>G	XP_016873561.1:n.-557+255027A>G
XM_017018073.2:c.-416+255027A>G	XP_016873562.1:n.-416+255027A>G
XM_017018075.2:c.-363+255027A>G	XP_016873564.1:n.-363+255027A>G
XM_017018077.2:c.-443+255027A>G	XP_016873566.1:n.-443+255027A>G
XM_017018079.2:c.-359+18393A>G	XP_016873568.1:n.-359+18393A>G
XM_024448626.1:c.-496+18393A>G	XP_024304394.1:n.-496+18393A>G
XM_024448627.1:c.-496+18393A>G	XP_024304395.1:n.-496+18393A>G
NM_001258419.2:c.-496+255027A>G MANE Select	NP_001245348.1:n.-496+255027A>G
NM_020929.3:c.-327+255027A>G	NP_065980.1:n.-327+255027A>G