Canonical Allele Identifier: CA411648728

Gene: ADSL

Linked Data

• MyVariant Identifiers: chr22:g.40761049G>T (hg19) ; chr22:g.40365045G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40365045G>T , CM000684.2:g.40365045G>T	GRCh38
NC_000022.10:g.40761049G>T , CM000684.1:g.40761049G>T	GRCh37
NC_000022.9:g.39090995G>T	NCBI36
NG_007993.1:g.23546G>T
NG_007993.2:g.23546G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*751G>T	ENSP00000485462.2:n.*751G>T
ENST00000623287.4:c.*782G>T	ENSP00000485437.1:n.*782G>T
ENST00000623632.4:c.1048G>T	ENSP00000485288.2:p.Ala350Ser
ENST00000625194.4:c.1399G>T	ENSP00000485289.2:p.Ala467Ser
ENST00000636433.1:n.1379G>T
ENST00000636714.1:c.1357G>T	ENSP00000490946.1:p.Ala453Ser
ENST00000637666.2:c.1191+680G>T	ENSP00000489696.2:n.1191+680G>T
ENST00000637669.1:c.1357G>T	ENSP00000489728.1:p.Ala453Ser
ENST00000639722.1:c.*1053G>T	ENSP00000492828.1:n.*1053G>T
ENST00000674592.1:n.2871G>T
ENST00000675622.1:n.4424G>T
ENST00000679609.1:c.*967G>T	ENSP00000506592.1:n.*967G>T
ENST00000679656.1:n.2042G>T
ENST00000679723.1:c.1312G>T	ENSP00000505155.1:p.Ala438Ser
ENST00000679845.1:n.1665G>T
ENST00000679904.1:n.1753G>T
ENST00000680378.1:c.1444G>T	ENSP00000505556.1:p.Ala482Ser
ENST00000680444.1:c.*720G>T	ENSP00000505298.1:n.*720G>T
ENST00000680978.1:c.1357G>T	ENSP00000505244.1:p.Ala453Ser
ENST00000681003.1:n.820G>T
ENST00000681159.1:n.2761G>T
ENST00000216194.11:c.1399G>T	ENSP00000216194.8:p.Ala467Ser
ENST00000342312.9:c.1191+680G>T	ENSP00000341429.6:n.1191+680G>T
ENST00000423176.6:c.84G>T
ENST00000498234.2:c.15G>T
ENST00000623063.3:c.1357G>T MANE Select	ENSP00000485525.1:p.Ala453Ser
ENST00000623387.1:n.488G>T
ENST00000623869.3:c.88G>T	ENSP00000485211.1:p.Ala30Ser
ENST00000624027.1:c.84G>T
ENST00000625194.3:c.986G>T
NM_000026.2:c.1357G>T	NP_000017.1:p.Ala453Ser
NM_001123378.1:c.1191+680G>T	NP_001116850.1:n.1191+680G>T
XM_011529976.1:c.1357G>T	XP_011528278.1:p.Ala453Ser
XM_011529977.1:c.1357G>T	XP_011528279.1:p.Ala453Ser
XM_011529978.1:c.1191+680G>T	XP_011528280.1:n.1191+680G>T
XM_011529979.1:c.1357G>T	XP_011528281.1:p.Ala453Ser
XM_011529980.1:c.1191+680G>T	XP_011528282.1:n.1191+680G>T
XM_011529981.1:c.892G>T	XP_011528283.1:p.Ala298Ser
XM_011529982.1:c.526G>T	XP_011528284.1:p.Ala176Ser
XR_937824.1:n.1447G>T
XR_937825.1:n.1281+680G>T
NM_000026.3:c.1357G>T	NP_000017.1:p.Ala453Ser
NM_001123378.2:c.1191+680G>T	NP_001116850.1:n.1191+680G>T
NM_001317923.1:c.1165G>T	NP_001304852.1:p.Ala389Ser
NM_001363840.1:c.1357G>T	NP_001350769.1:p.Ala453Ser
NR_134256.1:n.1447G>T
XM_011529977.3:c.1357G>T	XP_011528279.1:p.Ala453Ser
XM_011529980.3:c.1191+680G>T	XP_011528282.1:n.1191+680G>T
XM_017028636.1:c.1312G>T	XP_016884125.1:p.Ala438Ser
XM_017028637.1:c.1312G>T	XP_016884126.1:p.Ala438Ser
XM_017028638.1:c.892G>T	XP_016884127.1:p.Ala298Ser
XM_017028639.2:c.892G>T	XP_016884128.1:p.Ala298Ser
XM_017028640.1:c.526G>T	XP_016884129.1:p.Ala176Ser
XM_024452166.1:c.1146+680G>T	XP_024307934.1:n.1146+680G>T
XR_001755176.2:n.1599G>T
XR_002958670.1:n.1384G>T
XR_937825.3:n.1279+680G>T
NM_000026.4:c.1357G>T MANE Select	NP_000017.1:p.Ala453Ser
NM_001363840.2:c.1357G>T	NP_001350769.1:p.Ala453Ser
NM_001123378.3:c.1191+680G>T	NP_001116850.1:n.1191+680G>T
NM_001317923.2:c.1165G>T	NP_001304852.1:p.Ala389Ser
NM_001363840.3:c.1357G>T	NP_001350769.1:p.Ala453Ser
NR_134256.2:n.1447G>T