Canonical Allele Identifier: CA1979579386

Gene: PACS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66211217G= , CM000673.2:g.66211217G=	GRCh38
NC_000011.9:g.65978688G= , CM000673.1:g.65978688G=	GRCh37
NC_000011.8:g.65735264G=	NCBI36
NG_033900.1:g.145865G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320580.9:c.618G= MANE Select	ENSP00000316454.4:p.Leu206=
ENST00000320580.8:c.618G=	ENSP00000316454.4:p.Leu206=
ENST00000527224.1:n.742G=
ENST00000527380.1:c.324G=	ENSP00000432639.1:p.Leu108=
ENST00000533756.5:c.309G=	ENSP00000437150.1:p.Leu103=
NM_018026.3:c.618G=	NP_060496.2:p.Leu206=
XM_011545162.1:c.297G=	XP_011543464.1:p.Leu99=
XM_011545163.1:c.288G=	XP_011543465.1:p.Leu96=
XM_011545164.1:c.279G=	XP_011543466.1:p.Leu93=
XM_011545164.2:c.279G=	XP_011543466.1:p.Leu93=
XR_001747924.1:n.829G=
NM_018026.4:c.618G= MANE Select	NP_060496.2:p.Leu206=