Canonical Allele Identifier: CA362798455

Gene: MYLIP

Linked Data

• dbSNP Id: rs9370867
• MyVariant Identifiers: chr6:g.16145325A>C (hg19) ; chr6:g.16145094A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.16145094A>C , CM000668.2:g.16145094A>C	GRCh38
NC_000006.11:g.16145325A>C , CM000668.1:g.16145325A>C	GRCh37
NC_000006.10:g.16253304A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356840.8:c.1025A>C MANE Select	ENSP00000349298.3:p.Asn342Thr
ENST00000349606.4:c.482A>C	ENSP00000008686.5:p.Asn161Thr
ENST00000356840.7:c.1025A>C	ENSP00000349298.3:p.Asn342Thr
NM_013262.3:c.1025A>C	NP_037394.2:p.Asn342Thr
XM_005249032.2:c.860A>C	XP_005249089.1:p.Asn287Thr
XM_005249033.2:c.482A>C	XP_005249090.1:p.Asn161Thr
XM_005249033.3:c.482A>C	XP_005249090.1:p.Asn161Thr
XM_017010789.1:c.1025A>C	XP_016866278.1:p.Asn342Thr
NM_013262.4:c.1025A>C MANE Select	NP_037394.2:p.Asn342Thr