Canonical Allele Identifier: CA2410658333

Gene: MLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50084735C= , CM000684.2:g.50084735C=	GRCh38
NC_000022.10:g.50523164C= , CM000684.1:g.50523164C=	GRCh37
NC_000022.9:g.48865291C=	NCBI36
NG_009162.1:g.6195G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000311597.10:c.168G= MANE Select	ENSP00000310375.6:p.Val56=
ENST00000311597.9:c.168G=	ENSP00000310375.5:p.Val56=
ENST00000395876.6:c.168G=	ENSP00000379216.2:p.Val56=
ENST00000442311.1:c.168G=	ENSP00000401385.1:p.Val56=
NM_015166.3:c.168G=	NP_055981.1:p.Val56=
NM_139202.2:c.168G=	NP_631941.1:p.Val56=
XM_011530678.1:c.168G=	XP_011528980.1:p.Val56=
XR_430476.2:n.563G=
XM_011530678.2:c.168G=	XP_011528980.1:p.Val56=
XM_017028671.1:c.168G=	XP_016884160.1:p.Val56=
XR_001755180.2:n.673G=
XR_001755181.2:n.441G=
NM_001376472.1:c.168G=	NP_001363401.1:p.Val56=
NM_001376473.1:c.168G=	NP_001363402.1:p.Val56=
NM_001376474.1:c.168G=	NP_001363403.1:p.Val56=
NM_001376475.1:c.168G=	NP_001363404.1:p.Val56=
NM_001376476.1:c.168G=	NP_001363405.1:p.Val56=
NM_001376477.1:c.168G=	NP_001363406.1:p.Val56=
NM_001376478.1:c.168G=	NP_001363407.1:p.Val56=
NM_001376479.1:c.168G=	NP_001363408.1:p.Val56=
NM_001376480.1:c.168G=	NP_001363409.1:p.Val56=
NM_001376481.1:c.168G=	NP_001363410.1:p.Val56=
NM_001376482.1:c.168G=	NP_001363411.1:p.Val56=
NM_001376483.1:c.168G=	NP_001363412.1:p.Val56=
NM_001376484.1:c.-59+620G=	NP_001363413.1:n.-59+620G=
NM_015166.4:c.168G= MANE Select	NP_055981.1:p.Val56=
NM_139202.3:c.168G=	NP_631941.1:p.Val56=
NR_164811.1:n.515G=
NR_164812.1:n.299G=
NR_164813.1:n.692G=