Canonical Allele Identifier: CA391240869

Gene: ADSS1

Linked Data

• MyVariant Identifiers: chr14:g.105207581G>C (hg19) ; chr14:g.104741244G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104741244G>C , CM000676.2:g.104741244G>C	GRCh38
NC_000014.8:g.105207581G>C , CM000676.1:g.105207581G>C	GRCh37
NC_000014.7:g.104278626G>C	NCBI36
NG_051175.1:g.22048G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000710323.1:c.793+1G>C	ENSP00000518203.1:n.793+1G>C
ENST00000330877.7:c.793+1G>C MANE Select	ENSP00000331260.2:n.793+1G>C
ENST00000330877.6:c.793+1G>C	ENSP00000331260.2:n.793+1G>C
ENST00000332972.9:c.922+1G>C	ENSP00000333019.5:n.922+1G>C
ENST00000553540.5:c.905+1G>C	ENSP00000450759.1:n.905+1G>C
ENST00000555486.5:c.858+1G>C	ENSP00000473778.1:n.858+1G>C
ENST00000557582.5:n.1714+1G>C
NM_152328.3:c.793+1G>C	NP_689541.1:n.793+1G>C
NM_199165.1:c.922+1G>C	NP_954634.1:n.922+1G>C
XM_006720026.2:c.796+1G>C	XP_006720089.1:n.796+1G>C
XM_011536412.1:c.925+1G>C	XP_011534714.1:n.925+1G>C
XM_011536413.1:c.610+1G>C	XP_011534715.1:n.610+1G>C
XM_011536414.1:c.607+1G>C	XP_011534716.1:n.607+1G>C
XM_011536415.1:c.178+1G>C	XP_011534717.1:n.178+1G>C
NM_001320424.1:c.178+1G>C	NP_001307353.1:n.178+1G>C
NM_152328.4:c.793+1G>C	NP_689541.1:n.793+1G>C
NM_199165.2:c.922+1G>C	NP_954634.1:n.922+1G>C
XM_006720026.3:c.796+1G>C	XP_006720089.1:n.796+1G>C
XM_011536412.2:c.925+1G>C	XP_011534714.1:n.925+1G>C
XR_001750917.1:n.465C>G
NM_152328.5:c.793+1G>C MANE Select	NP_689541.1:n.793+1G>C