Canonical Allele Identifier: CA684581685

Linked Data

dbSNP Id: rs1416124423

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.122176286_122176287del , CM000674.2:g.122176286_122176287del GRCh38
NC_000012.11:g.122660833_122660834del , CM000674.1:g.122660833_122660834del GRCh37
NC_000012.10:g.121226786_121226787del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000537729.5:c.-405-8233_-405-8232del (LRRC43) ENSP00000438751.1:n.-405-8233_-405-8232de...
NM_152759.4:c.-405-8233_-405-8232del (LRRC43) NP_689972.3:n.-405-8233_-405-8232del
XM_011538326.1:c.-65-2049_-65-2048del (IL31) XP_011536628.1:n.-65-2049_-65-2048del
NM_152759.5:c.-405-8233_-405-8232del (LRRC43) NP_689972.3:n.-405-8233_-405-8232del