Canonical Allele Identifier: CA2410655814

Gene: MLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50079918G= , CM000684.2:g.50079918G=	GRCh38
NC_000022.10:g.50518347G= , CM000684.1:g.50518347G=	GRCh37
NC_000022.9:g.48860474G=	NCBI36
NG_009162.1:g.11012C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311597.10:c.423C= MANE Select	ENSP00000310375.6:p.Asn141=
ENST00000311597.9:c.423C=	ENSP00000310375.5:p.Asn141=
ENST00000395876.6:c.423C=	ENSP00000379216.2:p.Asn141=
ENST00000442311.1:c.333C=	ENSP00000401385.1:p.Asn111=
NM_015166.3:c.423C=	NP_055981.1:p.Asn141=
NM_139202.2:c.423C=	NP_631941.1:p.Asn141=
XM_011530678.1:c.423C=	XP_011528980.1:p.Asn141=
XR_430476.2:n.818C=
XM_011530678.2:c.423C=	XP_011528980.1:p.Asn141=
XM_017028671.1:c.423C=	XP_016884160.1:p.Asn141=
XR_001755180.2:n.928C=
XR_001755181.2:n.696C=
NM_001376472.1:c.423C=	NP_001363401.1:p.Asn141=
NM_001376473.1:c.423C=	NP_001363402.1:p.Asn141=
NM_001376474.1:c.423C=	NP_001363403.1:p.Asn141=
NM_001376475.1:c.423C=	NP_001363404.1:p.Asn141=
NM_001376476.1:c.423C=	NP_001363405.1:p.Asn141=
NM_001376477.1:c.423C=	NP_001363406.1:p.Asn141=
NM_001376478.1:c.423C=	NP_001363407.1:p.Asn141=
NM_001376479.1:c.423C=	NP_001363408.1:p.Asn141=
NM_001376480.1:c.333C=	NP_001363409.1:p.Asn111=
NM_001376481.1:c.321+426C=	NP_001363410.1:n.321+426C=
NM_001376482.1:c.268-2416C=	NP_001363411.1:n.268-2416C=
NM_001376483.1:c.268-2416C=	NP_001363412.1:n.268-2416C=
NM_001376484.1:c.186C=	NP_001363413.1:p.Asn62=
NM_015166.4:c.423C= MANE Select	NP_055981.1:p.Asn141=
NM_139202.3:c.423C=	NP_631941.1:p.Asn141=
NR_164811.1:n.770C=
NR_164812.1:n.554C=
NR_164813.1:n.947C=