Canonical Allele Identifier: CA2089027962
Gene: LRRC63 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46259582G>A , CM000675.2:g.46259582G>A GRCh38
NC_000013.10:g.46833717G>A , CM000675.1:g.46833717G>A GRCh37
NC_000013.9:g.45731718G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595396.3:c.1227-2327G>A MANE Select ENSP00000469337.1:n.1227-2327G>A
ENST00000595396.2:c.1227-2327G>A ENSP00000469337.1:n.1227-2327G>A
ENST00000378805.7:c.1227-2327G>A ENSP00000368082.3:n.1227-2327G>A
ENST00000446175.5:c.1227-2327G>A ENSP00000408828.2:n.1227-2327G>A
ENST00000595396.1:c.1227-2327G>A ENSP00000469337.1:n.1227-2327G>A
NM_001282460.1:c.1227-2327G>A NP_001269389.1:n.1227-2327G>A
XM_011534981.1:c.1364+2309G>A XP_011533283.1:n.1364+2309G>A
XM_011534982.1:c.1364+2309G>A XP_011533284.1:n.1364+2309G>A
XM_011534983.1:c.1364+2309G>A XP_011533285.1:n.1364+2309G>A
XM_011534984.1:c.1328+2309G>A XP_011533286.1:n.1328+2309G>A
XM_011534985.1:c.1214+2309G>A XP_011533287.1:n.1214+2309G>A
XM_011534986.1:c.686+2309G>A XP_011533288.1:n.686+2309G>A
XM_011534987.1:c.686+2309G>A XP_011533289.1:n.686+2309G>A
XM_011534988.1:c.650+2309G>A XP_011533290.1:n.650+2309G>A
XM_011534991.1:c.1090-2327G>A XP_011533293.1:n.1090-2327G>A
XM_011534992.1:c.1090-7151G>A XP_011533294.1:n.1090-7151G>A
XM_011534993.1:c.991-17008G>A XP_011533295.1:n.991-17008G>A
XR_941519.1:n.2104-2327G>A
NM_001282460.2:c.1227-2327G>A MANE Select NP_001269389.1:n.1227-2327G>A
XM_011534992.2:c.1090-7151G>A XP_011533294.1:n.1090-7151G>A
XM_017020421.1:c.1227-2327G>A XP_016875910.1:n.1227-2327G>A
XM_017020422.1:c.1191-2327G>A XP_016875911.1:n.1191-2327G>A
XM_017020423.1:c.1077-2327G>A XP_016875912.1:n.1077-2327G>A
XM_017020428.1:c.1090-7151G>A XP_016875917.1:n.1090-7151G>A
XM_017020429.1:c.549-2327G>A XP_016875918.1:n.549-2327G>A
XM_017020430.1:c.549-2327G>A XP_016875919.1:n.549-2327G>A
XM_017020431.1:c.513-2327G>A XP_016875920.1:n.513-2327G>A
XR_001749493.1:n.4887+2309G>A
XR_941519.2:n.2104-2327G>A