Canonical Allele Identifier: CA1612565365

Gene: MYLIP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.16145077G= , CM000668.2:g.16145077G=	GRCh38
NC_000006.11:g.16145308G= , CM000668.1:g.16145308G=	GRCh37
NC_000006.10:g.16253287G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356840.8:c.1008G= MANE Select	ENSP00000349298.3:p.Val336=
ENST00000349606.4:c.465G=	ENSP00000008686.5:p.Val155=
ENST00000356840.7:c.1008G=	ENSP00000349298.3:p.Val336=
NM_013262.3:c.1008G=	NP_037394.2:p.Val336=
XM_005249032.2:c.843G=	XP_005249089.1:p.Val281=
XM_005249033.2:c.465G=	XP_005249090.1:p.Val155=
XM_005249033.3:c.465G=	XP_005249090.1:p.Val155=
XM_017010789.1:c.1008G=	XP_016866278.1:p.Val336=
NM_013262.4:c.1008G= MANE Select	NP_037394.2:p.Val336=