Canonical Allele Identifier: CA1612565379

Gene: MYLIP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.16145089A= , CM000668.2:g.16145089A=	GRCh38
NC_000006.11:g.16145320A= , CM000668.1:g.16145320A=	GRCh37
NC_000006.10:g.16253299A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356840.8:c.1020A= MANE Select	ENSP00000349298.3:p.Ser340=
ENST00000349606.4:c.477A=	ENSP00000008686.5:p.Ser159=
ENST00000356840.7:c.1020A=	ENSP00000349298.3:p.Ser340=
NM_013262.3:c.1020A=	NP_037394.2:p.Ser340=
XM_005249032.2:c.855A=	XP_005249089.1:p.Ser285=
XM_005249033.2:c.477A=	XP_005249090.1:p.Ser159=
XM_005249033.3:c.477A=	XP_005249090.1:p.Ser159=
XM_017010789.1:c.1020A=	XP_016866278.1:p.Ser340=
NM_013262.4:c.1020A= MANE Select	NP_037394.2:p.Ser340=