Canonical Allele Identifier: CA411648348

Gene: ADSL

Linked Data

• MyVariant Identifiers: chr22:g.40760999T>A (hg19) ; chr22:g.40364995T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40364995T>A , CM000684.2:g.40364995T>A	GRCh38
NC_000022.10:g.40760999T>A , CM000684.1:g.40760999T>A	GRCh37
NC_000022.9:g.39090945T>A	NCBI36
NG_007993.1:g.23496T>A
NG_007993.2:g.23496T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480775.3:c.*701T>A	ENSP00000485462.2:n.*701T>A
ENST00000623287.4:c.*732T>A	ENSP00000485437.1:n.*732T>A
ENST00000623632.4:c.998T>A	ENSP00000485288.2:p.Ile333Asn
ENST00000625194.4:c.1349T>A	ENSP00000485289.2:p.Ile450Asn
ENST00000636433.1:n.1329T>A
ENST00000636714.1:c.1307T>A	ENSP00000490946.1:p.Ile436Asn
ENST00000637666.2:c.1191+630T>A	ENSP00000489696.2:n.1191+630T>A
ENST00000637669.1:c.1307T>A	ENSP00000489728.1:p.Ile436Asn
ENST00000639722.1:c.*1003T>A	ENSP00000492828.1:n.*1003T>A
ENST00000674592.1:n.2821T>A
ENST00000675622.1:n.4374T>A
ENST00000679609.1:c.*917T>A	ENSP00000506592.1:n.*917T>A
ENST00000679656.1:n.1992T>A
ENST00000679723.1:c.1262T>A	ENSP00000505155.1:p.Ile421Asn
ENST00000679845.1:n.1615T>A
ENST00000679904.1:n.1703T>A
ENST00000680378.1:c.1394T>A	ENSP00000505556.1:p.Ile465Asn
ENST00000680444.1:c.*670T>A	ENSP00000505298.1:n.*670T>A
ENST00000680978.1:c.1307T>A	ENSP00000505244.1:p.Ile436Asn
ENST00000681003.1:n.770T>A
ENST00000681159.1:n.2711T>A
ENST00000216194.11:c.1349T>A	ENSP00000216194.8:p.Ile450Asn
ENST00000342312.9:c.1191+630T>A	ENSP00000341429.6:n.1191+630T>A
ENST00000423176.6:c.34T>A
ENST00000623063.3:c.1307T>A MANE Select	ENSP00000485525.1:p.Ile436Asn
ENST00000623387.1:n.438T>A
ENST00000623869.3:c.38T>A	ENSP00000485211.1:p.Ile13Asn
ENST00000624027.1:c.34T>A
ENST00000625194.3:c.936T>A
NM_000026.2:c.1307T>A	NP_000017.1:p.Ile436Asn
NM_001123378.1:c.1191+630T>A	NP_001116850.1:n.1191+630T>A
XM_011529976.1:c.1307T>A	XP_011528278.1:p.Ile436Asn
XM_011529977.1:c.1307T>A	XP_011528279.1:p.Ile436Asn
XM_011529978.1:c.1191+630T>A	XP_011528280.1:n.1191+630T>A
XM_011529979.1:c.1307T>A	XP_011528281.1:p.Ile436Asn
XM_011529980.1:c.1191+630T>A	XP_011528282.1:n.1191+630T>A
XM_011529981.1:c.842T>A	XP_011528283.1:p.Ile281Asn
XM_011529982.1:c.476T>A	XP_011528284.1:p.Ile159Asn
XR_937824.1:n.1397T>A
XR_937825.1:n.1281+630T>A
NM_000026.3:c.1307T>A	NP_000017.1:p.Ile436Asn
NM_001123378.2:c.1191+630T>A	NP_001116850.1:n.1191+630T>A
NM_001317923.1:c.1115T>A	NP_001304852.1:p.Ile372Asn
NM_001363840.1:c.1307T>A	NP_001350769.1:p.Ile436Asn
NR_134256.1:n.1397T>A
XM_011529977.3:c.1307T>A	XP_011528279.1:p.Ile436Asn
XM_011529980.3:c.1191+630T>A	XP_011528282.1:n.1191+630T>A
XM_017028636.1:c.1262T>A	XP_016884125.1:p.Ile421Asn
XM_017028637.1:c.1262T>A	XP_016884126.1:p.Ile421Asn
XM_017028638.1:c.842T>A	XP_016884127.1:p.Ile281Asn
XM_017028639.2:c.842T>A	XP_016884128.1:p.Ile281Asn
XM_017028640.1:c.476T>A	XP_016884129.1:p.Ile159Asn
XM_024452166.1:c.1146+630T>A	XP_024307934.1:n.1146+630T>A
XR_001755176.2:n.1549T>A
XR_002958670.1:n.1334T>A
XR_937825.3:n.1279+630T>A
NM_000026.4:c.1307T>A MANE Select	NP_000017.1:p.Ile436Asn
NM_001363840.2:c.1307T>A	NP_001350769.1:p.Ile436Asn
NM_001123378.3:c.1191+630T>A	NP_001116850.1:n.1191+630T>A
NM_001317923.2:c.1115T>A	NP_001304852.1:p.Ile372Asn
NM_001363840.3:c.1307T>A	NP_001350769.1:p.Ile436Asn
NR_134256.2:n.1397T>A