Canonical Allele Identifier: CA616447738

Gene: ADSS1

Linked Data

• dbSNP Id: rs1470268018
• gnomAD v2: 14-105207368-G-A
• gnomAD v3: 14-104741031-G-A
• gnomAD v4: 14-104741031-G-A
• MyVariant Identifiers: chr14:g.105207368G>A (hg19) ; chr14:g.104741031G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104741031G>A , CM000676.2:g.104741031G>A	GRCh38
NC_000014.8:g.105207368G>A , CM000676.1:g.105207368G>A	GRCh37
NC_000014.7:g.104278413G>A	NCBI36
NG_051175.1:g.21835G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710323.1:c.667-86G>A	ENSP00000518203.1:n.667-86G>A
ENST00000330877.7:c.667-86G>A MANE Select	ENSP00000331260.2:n.667-86G>A
ENST00000330877.6:c.667-86G>A	ENSP00000331260.2:n.667-86G>A
ENST00000332972.9:c.796-86G>A	ENSP00000333019.5:n.796-86G>A
ENST00000553540.5:c.779-86G>A	ENSP00000450759.1:n.779-86G>A
ENST00000555486.5:c.732-86G>A	ENSP00000473778.1:n.732-86G>A
ENST00000557582.5:n.1588-86G>A
NM_152328.3:c.667-86G>A	NP_689541.1:n.667-86G>A
NM_199165.1:c.796-86G>A	NP_954634.1:n.796-86G>A
XM_006720026.2:c.670-86G>A	XP_006720089.1:n.670-86G>A
XM_011536412.1:c.799-86G>A	XP_011534714.1:n.799-86G>A
XM_011536413.1:c.484-86G>A	XP_011534715.1:n.484-86G>A
XM_011536414.1:c.481-86G>A	XP_011534716.1:n.481-86G>A
XM_011536415.1:c.52-86G>A	XP_011534717.1:n.52-86G>A
NM_001320424.1:c.52-86G>A	NP_001307353.1:n.52-86G>A
NM_152328.4:c.667-86G>A	NP_689541.1:n.667-86G>A
NM_199165.2:c.796-86G>A	NP_954634.1:n.796-86G>A
XM_006720026.3:c.670-86G>A	XP_006720089.1:n.670-86G>A
XM_011536412.2:c.799-86G>A	XP_011534714.1:n.799-86G>A
NM_152328.5:c.667-86G>A MANE Select	NP_689541.1:n.667-86G>A