Canonical Allele Identifier: CA446041933

Gene: LOX

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.122076955C>G , CM000667.2:g.122076955C>G	GRCh38
NC_000005.9:g.121412650C>G , CM000667.1:g.121412650C>G	GRCh37
NC_000005.8:g.121440549C>G	NCBI36
NG_008722.1:g.6406G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231004.5:c.678G>C MANE Select	ENSP00000231004.4:p.Thr226=
ENST00000639739.2:c.631+400G>C	ENSP00000492324.2:n.631+400G>C
ENST00000231004.4:c.678G>C	ENSP00000231004.4:p.Thr226=
ENST00000503759.5:n.269G>C
ENST00000508067.1:c.118+400G>C	ENSP00000427538.1:n.118+400G>C
ENST00000513319.5:n.83+137G>C
NM_001178102.1:c.-13G>C	NP_001171573.1:n.-13G>C
NM_001178102.2:c.-13G>C	NP_001171573.1:n.-13G>C
NM_001317073.1:c.-152+137G>C	NP_001304002.1:n.-152+137G>C
NM_002317.5:c.678G>C	NP_002308.2:p.Thr226=
NM_002317.6:c.678G>C	NP_002308.2:p.Thr226=
NM_002317.7:c.678G>C MANE Select	NP_002308.2:p.Thr226=