Canonical Allele Identifier: CA1332842835

Gene: COL4A3 MFF-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227266391_227266393delinsTTG , CM000664.2:g.227266391_227266393delinsTTG	GRCh38
NC_000002.11:g.228131107_228131109delinsTTG , CM000664.1:g.228131107_228131109delinsTTG	GRCh37
NC_000002.10:g.227839351_227839353delinsTTG	NCBI36
NG_011591.1:g.106827_106829delinsTTG , LRG_230:g.106827_106829delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396578.8:c.1316-26_1316-24delinsTTG (COL4A3) MANE Select	ENSP00000379823.3:n.1316-26_1316-24delinsTTG
ENST00000396578.7:c.1316-26_1316-24delinsTTG (COL4A3)	ENSP00000379823.3:n.1316-26_1316-24delinsTTG
NM_000091.4:c.1316-26_1316-24delinsTTG , LRG_230t1:c.1316-26_1316-24delinsTTG (COL4A3)	NP_000082.2:n.1316-26_1316-24delinsTTG
NR_102371.1:n.656-458_656-456delinsCAA (MFF-DT)
XM_005246276.2:c.1316-26_1316-24delinsTTG (COL4A3)	XP_005246333.1:n.1316-26_1316-24delinsTTG
XM_005246277.2:c.1316-26_1316-24delinsTTG (COL4A3)	XP_005246334.1:n.1316-26_1316-24delinsTTG
XM_005246280.2:c.1316-26_1316-24delinsTTG (COL4A3)	XP_005246337.1:n.1316-26_1316-24delinsTTG
XM_006712245.2:c.1316-26_1316-24delinsTTG (COL4A3)	XP_006712308.1:n.1316-26_1316-24delinsTTG
XM_011510555.1:c.1316-26_1316-24delinsTTG (COL4A3)	XP_011508857.1:n.1316-26_1316-24delinsTTG
XM_011510556.1:c.77-26_77-24delinsTTG (COL4A3)	XP_011508858.1:n.77-26_77-24delinsTTG
XR_241280.2:n.1454-26_1454-24delinsTTG (COL4A3)
XM_005246277.3:c.1316-26_1316-24delinsTTG (COL4A3)	XP_005246334.1:n.1316-26_1316-24delinsTTG
XM_005246280.3:c.1316-26_1316-24delinsTTG (COL4A3)	XP_005246337.1:n.1316-26_1316-24delinsTTG
XM_006712245.3:c.1316-26_1316-24delinsTTG (COL4A3)	XP_006712308.1:n.1316-26_1316-24delinsTTG
XM_011510556.2:c.77-26_77-24delinsTTG (COL4A3)	XP_011508858.1:n.77-26_77-24delinsTTG
XM_017003295.1:c.1316-26_1316-24delinsTTG (COL4A3)	XP_016858784.1:n.1316-26_1316-24delinsTTG
XR_001738601.1:n.1454-26_1454-24delinsTTG (COL4A3)
XR_241280.3:n.1454-26_1454-24delinsTTG (COL4A3)
NM_000091.5:c.1316-26_1316-24delinsTTG (COL4A3) MANE Select	NP_000082.2:n.1316-26_1316-24delinsTTG