Canonical Allele Identifier: CA913046853

Gene: AGL

Linked Data

• MyVariant Identifiers: chr1:g.100382268_100382271del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99916712_99916715del , CM000663.2:g.99916712_99916715del	GRCh38
NC_000001.10:g.100382268_100382271del , CM000663.1:g.100382268_100382271del	GRCh37
NC_000001.9:g.100154856_100154859del	NCBI36
NG_012865.1:g.71629_71632del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361915.8:c.4462_4465del MANE Select	ENSP00000355106.3:p.His1488MetfsTer15
ENST00000637337.1:n.4673_4676del
ENST00000294724.8:c.4462_4465del	ENSP00000294724.4:p.His1488MetfsTer15
ENST00000361302.7:c.4414_4417del	ENSP00000354971.3:p.His1472MetfsTer15
ENST00000361522.4:c.4411_4414del	ENSP00000354635.4:p.His1471MetfsTer15
ENST00000361915.7:c.4462_4465del	ENSP00000355106.3:p.His1488MetfsTer15
ENST00000370161.6:c.4414_4417del	ENSP00000359180.2:p.His1472MetfsTer15
ENST00000370163.7:c.4462_4465del	ENSP00000359182.3:p.His1488MetfsTer15
ENST00000370165.7:c.4462_4465del	ENSP00000359184.3:p.His1488MetfsTer15
NM_000028.2:c.4462_4465del	NP_000019.2:p.His1488MetfsTer15
NM_000642.2:c.4462_4465del	NP_000633.2:p.His1488MetfsTer15
NM_000643.2:c.4462_4465del	NP_000634.2:p.His1488MetfsTer15
NM_000644.2:c.4462_4465del	NP_000635.2:p.His1488MetfsTer15
NM_000645.2:c.4411_4414del	NP_000636.2:p.His1471MetfsTer15
NM_000646.2:c.4414_4417del	NP_000637.2:p.His1472MetfsTer15
XM_005270557.1:c.4462_4465del	XP_005270614.1:p.His1488MetfsTer15
XR_947626.1:n.1318-3498_1318-3495del
XR_947627.1:n.1207-3498_1207-3495del
XR_947628.1:n.1312-3498_1312-3495del
XR_947630.1:n.1250-3498_1250-3495del
XR_947632.1:n.1136-3498_1136-3495del
XR_947633.1:n.1247-3498_1247-3495del
XR_947634.1:n.661-3498_661-3495del
XR_947635.1:n.729-3498_729-3495del
XM_005270557.2:c.4462_4465del	XP_005270614.1:p.His1488MetfsTer15
XM_017000501.2:c.2722_2725del	XP_016855990.1:p.His908MetfsTer15
NM_000642.3:c.4462_4465del MANE Select	NP_000633.2:p.His1488MetfsTer15