Canonical Allele Identifier: CA391240848

Gene: ADSS1

Linked Data

• MyVariant Identifiers: chr14:g.105207577T>A (hg19) ; chr14:g.104741240T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104741240T>A , CM000676.2:g.104741240T>A	GRCh38
NC_000014.8:g.105207577T>A , CM000676.1:g.105207577T>A	GRCh37
NC_000014.7:g.104278622T>A	NCBI36
NG_051175.1:g.22044T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000710323.1:c.790T>A	ENSP00000518203.1:p.Phe264Ile
ENST00000330877.7:c.790T>A MANE Select	ENSP00000331260.2:p.Phe264Ile
ENST00000330877.6:c.790T>A	ENSP00000331260.2:p.Phe264Ile
ENST00000332972.9:c.919T>A	ENSP00000333019.5:p.Phe307Ile
ENST00000553540.5:c.902T>A	ENSP00000450759.1:n.902T>A
ENST00000555486.5:c.855T>A	ENSP00000473778.1:n.855T>A
ENST00000557582.5:n.1711T>A
NM_152328.3:c.790T>A	NP_689541.1:p.Phe264Ile
NM_199165.1:c.919T>A	NP_954634.1:p.Phe307Ile
XM_006720026.2:c.793T>A	XP_006720089.1:p.Phe265Ile
XM_011536412.1:c.922T>A	XP_011534714.1:p.Phe308Ile
XM_011536413.1:c.607T>A	XP_011534715.1:p.Phe203Ile
XM_011536414.1:c.604T>A	XP_011534716.1:p.Phe202Ile
XM_011536415.1:c.175T>A	XP_011534717.1:p.Phe59Ile
NM_001320424.1:c.175T>A	NP_001307353.1:p.Phe59Ile
NM_152328.4:c.790T>A	NP_689541.1:p.Phe264Ile
NM_199165.2:c.919T>A	NP_954634.1:p.Phe307Ile
XM_006720026.3:c.793T>A	XP_006720089.1:p.Phe265Ile
XM_011536412.2:c.922T>A	XP_011534714.1:p.Phe308Ile
XR_001750917.1:n.469A>T
NM_152328.5:c.790T>A MANE Select	NP_689541.1:p.Phe264Ile