Canonical Allele Identifier: CA381342477

Gene: PACS1

Linked Data

• MyVariant Identifiers: chr11:g.65978680A>T (hg19) ; chr11:g.66211209A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211209A>T , CM000673.2:g.66211209A>T	GRCh38
NC_000011.9:g.65978680A>T , CM000673.1:g.65978680A>T	GRCh37
NC_000011.8:g.65735256A>T	NCBI36
NG_033900.1:g.145857A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.610A>T MANE Select	ENSP00000316454.4:p.Thr204Ser
ENST00000320580.8:c.610A>T	ENSP00000316454.4:p.Thr204Ser
ENST00000527224.1:n.734A>T
ENST00000527380.1:c.316A>T	ENSP00000432639.1:p.Thr106Ser
ENST00000533756.5:c.301A>T	ENSP00000437150.1:p.Thr101Ser
NM_018026.3:c.610A>T	NP_060496.2:p.Thr204Ser
XM_011545162.1:c.289A>T	XP_011543464.1:p.Thr97Ser
XM_011545163.1:c.280A>T	XP_011543465.1:p.Thr94Ser
XM_011545164.1:c.271A>T	XP_011543466.1:p.Thr91Ser
XM_011545164.2:c.271A>T	XP_011543466.1:p.Thr91Ser
XR_001747924.1:n.821A>T
NM_018026.4:c.610A>T MANE Select	NP_060496.2:p.Thr204Ser