Canonical Allele Identifier: CA2410650180

Gene: MLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50068414G= , CM000684.2:g.50068414G=	GRCh38
NC_000022.10:g.50506843G= , CM000684.1:g.50506843G=	GRCh37
NC_000022.9:g.48848970G=	NCBI36
NG_009162.1:g.22516C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000311597.10:c.894+19C= MANE Select	ENSP00000310375.6:n.894+19C=
ENST00000311597.9:c.894+19C=	ENSP00000310375.5:n.894+19C=
ENST00000395876.6:c.894+19C=	ENSP00000379216.2:n.894+19C=
ENST00000483836.1:n.251+19C=
NM_015166.3:c.894+19C=	NP_055981.1:n.894+19C=
NM_139202.2:c.894+19C=	NP_631941.1:n.894+19C=
XM_011530678.1:c.894+19C=	XP_011528980.1:n.894+19C=
XR_430476.2:n.1289+19C=
XM_011530678.2:c.894+19C=	XP_011528980.1:n.894+19C=
XM_017028671.1:c.894+19C=	XP_016884160.1:n.894+19C=
XR_001755180.2:n.1399+19C=
XR_001755181.2:n.1167+19C=
NM_001376472.1:c.894+19C=	NP_001363401.1:n.894+19C=
NM_001376473.1:c.894+19C=	NP_001363402.1:n.894+19C=
NM_001376474.1:c.894+19C=	NP_001363403.1:n.894+19C=
NM_001376475.1:c.894+19C=	NP_001363404.1:n.894+19C=
NM_001376476.1:c.894+19C=	NP_001363405.1:n.894+19C=
NM_001376477.1:c.894+19C=	NP_001363406.1:n.894+19C=
NM_001376478.1:c.894+19C=	NP_001363407.1:n.894+19C=
NM_001376479.1:c.837+19C=	NP_001363408.1:n.837+19C=
NM_001376480.1:c.804+19C=	NP_001363409.1:n.804+19C=
NM_001376481.1:c.792+19C=	NP_001363410.1:n.792+19C=
NM_001376482.1:c.738+19C=	NP_001363411.1:n.738+19C=
NM_001376483.1:c.738+19C=	NP_001363412.1:n.738+19C=
NM_001376484.1:c.657+19C=	NP_001363413.1:n.657+19C=
NM_015166.4:c.894+19C= MANE Select	NP_055981.1:n.894+19C=
NM_139202.3:c.894+19C=	NP_631941.1:n.894+19C=
NR_164811.1:n.1241+19C=
NR_164812.1:n.1025+19C=
NR_164813.1:n.1418+19C=