Canonical Allele Identifier: CA362798387

Gene: MYLIP

Linked Data

• MyVariant Identifiers: chr6:g.16145312C>G (hg19) ; chr6:g.16145081C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.16145081C>G , CM000668.2:g.16145081C>G	GRCh38
NC_000006.11:g.16145312C>G , CM000668.1:g.16145312C>G	GRCh37
NC_000006.10:g.16253291C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356840.8:c.1012C>G MANE Select	ENSP00000349298.3:p.Leu338Val
ENST00000349606.4:c.469C>G	ENSP00000008686.5:p.Leu157Val
ENST00000356840.7:c.1012C>G	ENSP00000349298.3:p.Leu338Val
NM_013262.3:c.1012C>G	NP_037394.2:p.Leu338Val
XM_005249032.2:c.847C>G	XP_005249089.1:p.Leu283Val
XM_005249033.2:c.469C>G	XP_005249090.1:p.Leu157Val
XM_005249033.3:c.469C>G	XP_005249090.1:p.Leu157Val
XM_017010789.1:c.1012C>G	XP_016866278.1:p.Leu338Val
NM_013262.4:c.1012C>G MANE Select	NP_037394.2:p.Leu338Val