Canonical Allele Identifier: CA793602762

Gene: ADD1

Linked Data

• dbSNP Id: rs1164777290
• gnomAD v3: 4-2866811-C-G
• gnomAD v4: 4-2866811-C-G
• MyVariant Identifiers: chr4:g.2868538C>G (hg19) ; chr4:g.2866811C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.2866811C>G , CM000666.2:g.2866811C>G	GRCh38
NC_000004.11:g.2868538C>G , CM000666.1:g.2868538C>G	GRCh37
NC_000004.10:g.2838336C>G	NCBI36
NG_012037.1:g.27955C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000683351.1:c.-20-9085C>G MANE Select	ENSP00000508142.1:n.-20-9085C>G
ENST00000651918.1:c.-141-6204C>G	ENSP00000498269.1:n.-141-6204C>G
ENST00000264758.11:c.-20-9085C>G	ENSP00000264758.6:n.-20-9085C>G
ENST00000355842.7:c.-178-1161C>G	ENSP00000348100.3:n.-178-1161C>G
ENST00000374281.2:n.322-1161C>G
ENST00000398125.5:c.-20-9085C>G	ENSP00000381193.1:n.-20-9085C>G
ENST00000446856.5:c.-20-9085C>G	ENSP00000399828.2:n.-20-9085C>G
ENST00000503455.6:c.-20-9085C>G	ENSP00000423024.2:n.-20-9085C>G
ENST00000508277.5:c.-20-9085C>G	ENSP00000426700.1:n.-20-9085C>G
ENST00000508684.5:n.169-9085C>G
ENST00000509039.5:n.47-9085C>G
ENST00000510101.5:c.-20-9085C>G	ENSP00000425703.1:n.-20-9085C>G
ENST00000511797.5:c.-178-1161C>G	ENSP00000421918.1:n.-178-1161C>G
ENST00000513328.6:c.-20-9085C>G	ENSP00000421907.2:n.-20-9085C>G
ENST00000540541.1:n.37-9085C>G
NM_001119.4:c.-20-9085C>G	NP_001110.2:n.-20-9085C>G
NM_001286645.1:c.-178-1161C>G	NP_001273574.1:n.-178-1161C>G
NM_014189.3:c.-20-9085C>G	NP_054908.2:n.-20-9085C>G
NM_014190.3:c.-20-9085C>G	NP_054909.2:n.-20-9085C>G
NM_176801.2:c.-20-9085C>G	NP_789771.1:n.-20-9085C>G
XM_005247933.1:c.-20-9085C>G	XP_005247990.1:n.-20-9085C>G
XM_005247935.1:c.-20-9085C>G	XP_005247992.1:n.-20-9085C>G
XM_005247936.1:c.-20-9085C>G	XP_005247993.1:n.-20-9085C>G
XM_005247937.1:c.-20-9085C>G	XP_005247994.1:n.-20-9085C>G
NM_001354754.1:c.-21+6856C>G	NP_001341683.1:n.-21+6856C>G
NM_001354755.1:c.-20-9085C>G	NP_001341684.1:n.-20-9085C>G
NM_001354756.1:c.-20-9085C>G	NP_001341685.1:n.-20-9085C>G
NM_001354757.1:c.-21+6856C>G	NP_001341686.1:n.-21+6856C>G
NM_001354758.1:c.-20-9085C>G	NP_001341687.1:n.-20-9085C>G
NM_001354759.1:c.-20-9085C>G	NP_001341688.1:n.-20-9085C>G
NM_001354761.1:c.-20-9085C>G	NP_001341690.1:n.-20-9085C>G
NM_001354762.1:c.-20-9085C>G	NP_001341691.1:n.-20-9085C>G
XM_017007703.1:c.-21+6856C>G	XP_016863192.1:n.-21+6856C>G
XR_002959706.1:n.47-9085C>G
NM_001119.5:c.-20-9085C>G	NP_001110.2:n.-20-9085C>G
NM_001354754.2:c.-21+6856C>G	NP_001341683.1:n.-21+6856C>G
NM_001354756.2:c.-20-9085C>G	NP_001341685.1:n.-20-9085C>G
NM_001354757.2:c.-21+6856C>G	NP_001341686.1:n.-21+6856C>G
NM_001354759.2:c.-20-9085C>G	NP_001341688.1:n.-20-9085C>G
NM_001354761.2:c.-20-9085C>G MANE Select	NP_001341690.1:n.-20-9085C>G
NM_001354762.2:c.-20-9085C>G	NP_001341691.1:n.-20-9085C>G
NM_014190.4:c.-20-9085C>G	NP_054909.2:n.-20-9085C>G
NM_001286645.2:c.-178-1161C>G	NP_001273574.1:n.-178-1161C>G
NM_001354755.2:c.-20-9085C>G	NP_001341684.1:n.-20-9085C>G
NM_001354758.2:c.-20-9085C>G	NP_001341687.1:n.-20-9085C>G
NM_014189.4:c.-20-9085C>G	NP_054908.2:n.-20-9085C>G
NM_176801.3:c.-20-9085C>G	NP_789771.1:n.-20-9085C>G