Canonical Allele Identifier: CA2089181191

Gene: LRCH1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46593697A= , CM000675.2:g.46593697A=	GRCh38
NC_000013.10:g.47167832A= , CM000675.1:g.47167832A=	GRCh37
NC_000013.9:g.46065833A=	NCBI36
NG_021335.1:g.45537A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389797.8:c.307+39994A= MANE Select	ENSP00000374447.3:n.307+39994A=
ENST00000311191.10:c.307+39994A=	ENSP00000308493.5:n.307+39994A=
ENST00000389797.7:c.307+39994A=	ENSP00000374447.3:n.307+39994A=
ENST00000389798.7:c.307+39994A=	ENSP00000374448.3:n.307+39994A=
ENST00000443945.6:n.534+39994A=
NM_001164211.1:c.307+39994A=	NP_001157683.1:n.307+39994A=
NM_001164213.1:c.307+39994A=	NP_001157685.1:n.307+39994A=
NM_015116.2:c.307+39994A=	NP_055931.1:n.307+39994A=
XM_011535013.1:c.307+39994A=	XP_011533315.1:n.307+39994A=
XM_017020483.2:c.307+39994A=	XP_016875972.1:n.307+39994A=
XM_017020484.1:c.-329+39994A=	XP_016875973.1:n.-329+39994A=
XR_001749525.2:n.534+39994A=
NM_001164211.2:c.307+39994A= MANE Select	NP_001157683.2:n.307+39994A=
NM_001164213.2:c.307+39994A=	NP_001157685.2:n.307+39994A=
NM_015116.3:c.307+39994A=	NP_055931.2:n.307+39994A=