Canonical Allele Identifier: CA2089181292

Gene: LRCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46593855_46593856delinsGT , CM000675.2:g.46593855_46593856delinsGT	GRCh38
NC_000013.10:g.47167990_47167991delinsGT , CM000675.1:g.47167990_47167991delinsGT	GRCh37
NC_000013.9:g.46065991_46065992delinsGT	NCBI36
NG_021335.1:g.45695_45696delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000389797.8:c.307+40152_307+40153delinsGT MANE Select	ENSP00000374447.3:n.307+40152_307+40153delinsGT
ENST00000311191.10:c.307+40152_307+40153delinsGT	ENSP00000308493.5:n.307+40152_307+40153delinsGT
ENST00000389797.7:c.307+40152_307+40153delinsGT	ENSP00000374447.3:n.307+40152_307+40153delinsGT
ENST00000389798.7:c.307+40152_307+40153delinsGT	ENSP00000374448.3:n.307+40152_307+40153delinsGT
ENST00000443945.6:n.534+40152_534+40153delinsGT
NM_001164211.1:c.307+40152_307+40153delinsGT	NP_001157683.1:n.307+40152_307+40153delinsGT
NM_001164213.1:c.307+40152_307+40153delinsGT	NP_001157685.1:n.307+40152_307+40153delinsGT
NM_015116.2:c.307+40152_307+40153delinsGT	NP_055931.1:n.307+40152_307+40153delinsGT
XM_011535013.1:c.307+40152_307+40153delinsGT	XP_011533315.1:n.307+40152_307+40153delinsGT
XM_017020483.2:c.307+40152_307+40153delinsGT	XP_016875972.1:n.307+40152_307+40153delinsGT
XM_017020484.1:c.-329+40152_-329+40153delinsGT	XP_016875973.1:n.-329+40152_-329+40153delinsGT
XR_001749525.2:n.534+40152_534+40153delinsGT
NM_001164211.2:c.307+40152_307+40153delinsGT MANE Select	NP_001157683.2:n.307+40152_307+40153delinsGT
NM_001164213.2:c.307+40152_307+40153delinsGT	NP_001157685.2:n.307+40152_307+40153delinsGT
NM_015116.3:c.307+40152_307+40153delinsGT	NP_055931.2:n.307+40152_307+40153delinsGT