Canonical Allele Identifier: CA381342623

Gene: PACS1

Linked Data

• MyVariant Identifiers: chr11:g.65978690G>C (hg19) ; chr11:g.66211219G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211219G>C , CM000673.2:g.66211219G>C	GRCh38
NC_000011.9:g.65978690G>C , CM000673.1:g.65978690G>C	GRCh37
NC_000011.8:g.65735266G>C	NCBI36
NG_033900.1:g.145867G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.620G>C MANE Select	ENSP00000316454.4:p.Gly207Ala
ENST00000320580.8:c.620G>C	ENSP00000316454.4:p.Gly207Ala
ENST00000527224.1:n.744G>C
ENST00000527380.1:c.326G>C	ENSP00000432639.1:p.Gly109Ala
ENST00000533756.5:c.311G>C	ENSP00000437150.1:p.Gly104Ala
NM_018026.3:c.620G>C	NP_060496.2:p.Gly207Ala
XM_011545162.1:c.299G>C	XP_011543464.1:p.Gly100Ala
XM_011545163.1:c.290G>C	XP_011543465.1:p.Gly97Ala
XM_011545164.1:c.281G>C	XP_011543466.1:p.Gly94Ala
XM_011545164.2:c.281G>C	XP_011543466.1:p.Gly94Ala
XR_001747924.1:n.831G>C
NM_018026.4:c.620G>C MANE Select	NP_060496.2:p.Gly207Ala