Canonical Allele Identifier: CA2573158438

Gene: ADSL

Linked Data

• ClinVar Variation Id: 1482386
• ClinVar RCV Id: RCV002002918
• dbSNP Id: rs2146674336

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40365060A>C , CM000684.2:g.40365060A>C	GRCh38
NC_000022.10:g.40761064A>C , CM000684.1:g.40761064A>C	GRCh37
NC_000022.9:g.39091010A>C	NCBI36
NG_007993.1:g.23561A>C
NG_007993.2:g.23561A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*762+4A>C	ENSP00000485462.2:n.*762+4A>C
ENST00000623287.4:c.*793+4A>C	ENSP00000485437.1:n.*793+4A>C
ENST00000623632.4:c.1059+4A>C	ENSP00000485288.2:n.1059+4A>C
ENST00000625194.4:c.1410+4A>C	ENSP00000485289.2:n.1410+4A>C
ENST00000636433.1:n.1390+4A>C
ENST00000636714.1:c.1368+4A>C	ENSP00000490946.1:n.1368+4A>C
ENST00000637666.2:c.1191+695A>C	ENSP00000489696.2:n.1191+695A>C
ENST00000637669.1:c.1368+4A>C	ENSP00000489728.1:n.1368+4A>C
ENST00000639722.1:c.*1064+4A>C	ENSP00000492828.1:n.*1064+4A>C
ENST00000674592.1:n.2882+4A>C
ENST00000675622.1:n.4435+4A>C
ENST00000679609.1:c.*978+4A>C	ENSP00000506592.1:n.*978+4A>C
ENST00000679656.1:n.2053+4A>C
ENST00000679723.1:c.1323+4A>C	ENSP00000505155.1:n.1323+4A>C
ENST00000679845.1:n.1676+4A>C
ENST00000679904.1:n.1764+4A>C
ENST00000680378.1:c.1455+4A>C	ENSP00000505556.1:n.1455+4A>C
ENST00000680444.1:c.*731+4A>C	ENSP00000505298.1:n.*731+4A>C
ENST00000680978.1:c.1368+4A>C	ENSP00000505244.1:n.1368+4A>C
ENST00000681003.1:n.831+4A>C
ENST00000681159.1:n.2772+4A>C
ENST00000216194.11:c.1410+4A>C	ENSP00000216194.8:n.1410+4A>C
ENST00000342312.9:c.1191+695A>C	ENSP00000341429.6:n.1191+695A>C
ENST00000423176.6:c.95+4A>C
ENST00000498234.2:c.26+4A>C
ENST00000623063.3:c.1368+4A>C MANE Select	ENSP00000485525.1:n.1368+4A>C
ENST00000623387.1:n.499+4A>C
ENST00000623869.3:c.99+4A>C	ENSP00000485211.1:n.99+4A>C
ENST00000624027.1:c.95+4A>C
ENST00000625194.3:c.997+4A>C
NM_000026.2:c.1368+4A>C	NP_000017.1:n.1368+4A>C
NM_001123378.1:c.1191+695A>C	NP_001116850.1:n.1191+695A>C
XM_011529976.1:c.1368+4A>C	XP_011528278.1:n.1368+4A>C
XM_011529977.1:c.1368+4A>C	XP_011528279.1:n.1368+4A>C
XM_011529978.1:c.1191+695A>C	XP_011528280.1:n.1191+695A>C
XM_011529979.1:c.1368+4A>C	XP_011528281.1:n.1368+4A>C
XM_011529980.1:c.1191+695A>C	XP_011528282.1:n.1191+695A>C
XM_011529981.1:c.903+4A>C	XP_011528283.1:n.903+4A>C
XM_011529982.1:c.537+4A>C	XP_011528284.1:n.537+4A>C
XR_937824.1:n.1458+4A>C
XR_937825.1:n.1281+695A>C
NM_000026.3:c.1368+4A>C	NP_000017.1:n.1368+4A>C
NM_001123378.2:c.1191+695A>C	NP_001116850.1:n.1191+695A>C
NM_001317923.1:c.1176+4A>C	NP_001304852.1:n.1176+4A>C
NM_001363840.1:c.1368+4A>C	NP_001350769.1:n.1368+4A>C
NR_134256.1:n.1458+4A>C
XM_011529977.3:c.1368+4A>C	XP_011528279.1:n.1368+4A>C
XM_011529980.3:c.1191+695A>C	XP_011528282.1:n.1191+695A>C
XM_017028636.1:c.1323+4A>C	XP_016884125.1:n.1323+4A>C
XM_017028637.1:c.1323+4A>C	XP_016884126.1:n.1323+4A>C
XM_017028638.1:c.903+4A>C	XP_016884127.1:n.903+4A>C
XM_017028639.2:c.903+4A>C	XP_016884128.1:n.903+4A>C
XM_017028640.1:c.537+4A>C	XP_016884129.1:n.537+4A>C
XM_024452166.1:c.1146+695A>C	XP_024307934.1:n.1146+695A>C
XR_001755176.2:n.1610+4A>C
XR_002958670.1:n.1395+4A>C
XR_937825.3:n.1279+695A>C
NM_000026.4:c.1368+4A>C MANE Select	NP_000017.1:n.1368+4A>C
NM_001363840.2:c.1368+4A>C	NP_001350769.1:n.1368+4A>C
NM_001123378.3:c.1191+695A>C	NP_001116850.1:n.1191+695A>C
NM_001317923.2:c.1176+4A>C	NP_001304852.1:n.1176+4A>C
NM_001363840.3:c.1368+4A>C	NP_001350769.1:n.1368+4A>C
NR_134256.2:n.1458+4A>C