Canonical Allele Identifier: CA381342552

Gene: PACS1

Linked Data

• MyVariant Identifiers: chr11:g.65978686T>A (hg19) ; chr11:g.66211215T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211215T>A , CM000673.2:g.66211215T>A	GRCh38
NC_000011.9:g.65978686T>A , CM000673.1:g.65978686T>A	GRCh37
NC_000011.8:g.65735262T>A	NCBI36
NG_033900.1:g.145863T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.616T>A MANE Select	ENSP00000316454.4:p.Leu206Met
ENST00000320580.8:c.616T>A	ENSP00000316454.4:p.Leu206Met
ENST00000527224.1:n.740T>A
ENST00000527380.1:c.322T>A	ENSP00000432639.1:p.Leu108Met
ENST00000533756.5:c.307T>A	ENSP00000437150.1:p.Leu103Met
NM_018026.3:c.616T>A	NP_060496.2:p.Leu206Met
XM_011545162.1:c.295T>A	XP_011543464.1:p.Leu99Met
XM_011545163.1:c.286T>A	XP_011543465.1:p.Leu96Met
XM_011545164.1:c.277T>A	XP_011543466.1:p.Leu93Met
XM_011545164.2:c.277T>A	XP_011543466.1:p.Leu93Met
XR_001747924.1:n.827T>A
NM_018026.4:c.616T>A MANE Select	NP_060496.2:p.Leu206Met