Canonical Allele Identifier: CA411648567

Gene: ADSL

Linked Data

• MyVariant Identifiers: chr22:g.40761028C>G (hg19) ; chr22:g.40365024C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40365024C>G , CM000684.2:g.40365024C>G	GRCh38
NC_000022.10:g.40761028C>G , CM000684.1:g.40761028C>G	GRCh37
NC_000022.9:g.39090974C>G	NCBI36
NG_007993.1:g.23525C>G
NG_007993.2:g.23525C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*730C>G	ENSP00000485462.2:n.*730C>G
ENST00000623287.4:c.*761C>G	ENSP00000485437.1:n.*761C>G
ENST00000623632.4:c.1027C>G	ENSP00000485288.2:p.Pro343Ala
ENST00000625194.4:c.1378C>G	ENSP00000485289.2:p.Pro460Ala
ENST00000636433.1:n.1358C>G
ENST00000636714.1:c.1336C>G	ENSP00000490946.1:p.Pro446Ala
ENST00000637666.2:c.1191+659C>G	ENSP00000489696.2:n.1191+659C>G
ENST00000637669.1:c.1336C>G	ENSP00000489728.1:p.Pro446Ala
ENST00000639722.1:c.*1032C>G	ENSP00000492828.1:n.*1032C>G
ENST00000674592.1:n.2850C>G
ENST00000675622.1:n.4403C>G
ENST00000679609.1:c.*946C>G	ENSP00000506592.1:n.*946C>G
ENST00000679656.1:n.2021C>G
ENST00000679723.1:c.1291C>G	ENSP00000505155.1:p.Pro431Ala
ENST00000679845.1:n.1644C>G
ENST00000679904.1:n.1732C>G
ENST00000680378.1:c.1423C>G	ENSP00000505556.1:p.Pro475Ala
ENST00000680444.1:c.*699C>G	ENSP00000505298.1:n.*699C>G
ENST00000680978.1:c.1336C>G	ENSP00000505244.1:p.Pro446Ala
ENST00000681003.1:n.799C>G
ENST00000681159.1:n.2740C>G
ENST00000216194.11:c.1378C>G	ENSP00000216194.8:p.Pro460Ala
ENST00000342312.9:c.1191+659C>G	ENSP00000341429.6:n.1191+659C>G
ENST00000423176.6:c.63C>G
ENST00000623063.3:c.1336C>G MANE Select	ENSP00000485525.1:p.Pro446Ala
ENST00000623387.1:n.467C>G
ENST00000623869.3:c.67C>G	ENSP00000485211.1:p.Pro23Ala
ENST00000624027.1:c.63C>G
ENST00000625194.3:c.965C>G
NM_000026.2:c.1336C>G	NP_000017.1:p.Pro446Ala
NM_001123378.1:c.1191+659C>G	NP_001116850.1:n.1191+659C>G
XM_011529976.1:c.1336C>G	XP_011528278.1:p.Pro446Ala
XM_011529977.1:c.1336C>G	XP_011528279.1:p.Pro446Ala
XM_011529978.1:c.1191+659C>G	XP_011528280.1:n.1191+659C>G
XM_011529979.1:c.1336C>G	XP_011528281.1:p.Pro446Ala
XM_011529980.1:c.1191+659C>G	XP_011528282.1:n.1191+659C>G
XM_011529981.1:c.871C>G	XP_011528283.1:p.Pro291Ala
XM_011529982.1:c.505C>G	XP_011528284.1:p.Pro169Ala
XR_937824.1:n.1426C>G
XR_937825.1:n.1281+659C>G
NM_000026.3:c.1336C>G	NP_000017.1:p.Pro446Ala
NM_001123378.2:c.1191+659C>G	NP_001116850.1:n.1191+659C>G
NM_001317923.1:c.1144C>G	NP_001304852.1:p.Pro382Ala
NM_001363840.1:c.1336C>G	NP_001350769.1:p.Pro446Ala
NR_134256.1:n.1426C>G
XM_011529977.3:c.1336C>G	XP_011528279.1:p.Pro446Ala
XM_011529980.3:c.1191+659C>G	XP_011528282.1:n.1191+659C>G
XM_017028636.1:c.1291C>G	XP_016884125.1:p.Pro431Ala
XM_017028637.1:c.1291C>G	XP_016884126.1:p.Pro431Ala
XM_017028638.1:c.871C>G	XP_016884127.1:p.Pro291Ala
XM_017028639.2:c.871C>G	XP_016884128.1:p.Pro291Ala
XM_017028640.1:c.505C>G	XP_016884129.1:p.Pro169Ala
XM_024452166.1:c.1146+659C>G	XP_024307934.1:n.1146+659C>G
XR_001755176.2:n.1578C>G
XR_002958670.1:n.1363C>G
XR_937825.3:n.1279+659C>G
NM_000026.4:c.1336C>G MANE Select	NP_000017.1:p.Pro446Ala
NM_001363840.2:c.1336C>G	NP_001350769.1:p.Pro446Ala
NM_001123378.3:c.1191+659C>G	NP_001116850.1:n.1191+659C>G
NM_001317923.2:c.1144C>G	NP_001304852.1:p.Pro382Ala
NM_001363840.3:c.1336C>G	NP_001350769.1:p.Pro446Ala
NR_134256.2:n.1426C>G