Canonical Allele Identifier: CA411648672

Gene: ADSL

Linked Data

• MyVariant Identifiers: chr22:g.40761041C>A (hg19) ; chr22:g.40365037C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40365037C>A , CM000684.2:g.40365037C>A	GRCh38
NC_000022.10:g.40761041C>A , CM000684.1:g.40761041C>A	GRCh37
NC_000022.9:g.39090987C>A	NCBI36
NG_007993.1:g.23538C>A
NG_007993.2:g.23538C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*743C>A	ENSP00000485462.2:n.*743C>A
ENST00000623287.4:c.*774C>A	ENSP00000485437.1:n.*774C>A
ENST00000623632.4:c.1040C>A	ENSP00000485288.2:p.Thr347Asn
ENST00000625194.4:c.1391C>A	ENSP00000485289.2:p.Thr464Asn
ENST00000636433.1:n.1371C>A
ENST00000636714.1:c.1349C>A	ENSP00000490946.1:p.Thr450Asn
ENST00000637666.2:c.1191+672C>A	ENSP00000489696.2:n.1191+672C>A
ENST00000637669.1:c.1349C>A	ENSP00000489728.1:p.Thr450Asn
ENST00000639722.1:c.*1045C>A	ENSP00000492828.1:n.*1045C>A
ENST00000674592.1:n.2863C>A
ENST00000675622.1:n.4416C>A
ENST00000679609.1:c.*959C>A	ENSP00000506592.1:n.*959C>A
ENST00000679656.1:n.2034C>A
ENST00000679723.1:c.1304C>A	ENSP00000505155.1:p.Thr435Asn
ENST00000679845.1:n.1657C>A
ENST00000679904.1:n.1745C>A
ENST00000680378.1:c.1436C>A	ENSP00000505556.1:p.Thr479Asn
ENST00000680444.1:c.*712C>A	ENSP00000505298.1:n.*712C>A
ENST00000680978.1:c.1349C>A	ENSP00000505244.1:p.Thr450Asn
ENST00000681003.1:n.812C>A
ENST00000681159.1:n.2753C>A
ENST00000216194.11:c.1391C>A	ENSP00000216194.8:p.Thr464Asn
ENST00000342312.9:c.1191+672C>A	ENSP00000341429.6:n.1191+672C>A
ENST00000423176.6:c.76C>A
ENST00000498234.2:c.7C>A
ENST00000623063.3:c.1349C>A MANE Select	ENSP00000485525.1:p.Thr450Asn
ENST00000623387.1:n.480C>A
ENST00000623869.3:c.80C>A	ENSP00000485211.1:p.Thr27Asn
ENST00000624027.1:c.76C>A
ENST00000625194.3:c.978C>A
NM_000026.2:c.1349C>A	NP_000017.1:p.Thr450Asn
NM_001123378.1:c.1191+672C>A	NP_001116850.1:n.1191+672C>A
XM_011529976.1:c.1349C>A	XP_011528278.1:p.Thr450Asn
XM_011529977.1:c.1349C>A	XP_011528279.1:p.Thr450Asn
XM_011529978.1:c.1191+672C>A	XP_011528280.1:n.1191+672C>A
XM_011529979.1:c.1349C>A	XP_011528281.1:p.Thr450Asn
XM_011529980.1:c.1191+672C>A	XP_011528282.1:n.1191+672C>A
XM_011529981.1:c.884C>A	XP_011528283.1:p.Thr295Asn
XM_011529982.1:c.518C>A	XP_011528284.1:p.Thr173Asn
XR_937824.1:n.1439C>A
XR_937825.1:n.1281+672C>A
NM_000026.3:c.1349C>A	NP_000017.1:p.Thr450Asn
NM_001123378.2:c.1191+672C>A	NP_001116850.1:n.1191+672C>A
NM_001317923.1:c.1157C>A	NP_001304852.1:p.Thr386Asn
NM_001363840.1:c.1349C>A	NP_001350769.1:p.Thr450Asn
NR_134256.1:n.1439C>A
XM_011529977.3:c.1349C>A	XP_011528279.1:p.Thr450Asn
XM_011529980.3:c.1191+672C>A	XP_011528282.1:n.1191+672C>A
XM_017028636.1:c.1304C>A	XP_016884125.1:p.Thr435Asn
XM_017028637.1:c.1304C>A	XP_016884126.1:p.Thr435Asn
XM_017028638.1:c.884C>A	XP_016884127.1:p.Thr295Asn
XM_017028639.2:c.884C>A	XP_016884128.1:p.Thr295Asn
XM_017028640.1:c.518C>A	XP_016884129.1:p.Thr173Asn
XM_024452166.1:c.1146+672C>A	XP_024307934.1:n.1146+672C>A
XR_001755176.2:n.1591C>A
XR_002958670.1:n.1376C>A
XR_937825.3:n.1279+672C>A
NM_000026.4:c.1349C>A MANE Select	NP_000017.1:p.Thr450Asn
NM_001363840.2:c.1349C>A	NP_001350769.1:p.Thr450Asn
NM_001123378.3:c.1191+672C>A	NP_001116850.1:n.1191+672C>A
NM_001317923.2:c.1157C>A	NP_001304852.1:p.Thr386Asn
NM_001363840.3:c.1349C>A	NP_001350769.1:p.Thr450Asn
NR_134256.2:n.1439C>A