Canonical Allele Identifier: CA66608727

Gene: COL4A3 MFF-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227294547C>A , CM000664.2:g.227294547C>A	GRCh38
NC_000002.11:g.228159263C>A , CM000664.1:g.228159263C>A	GRCh37
NC_000002.10:g.227867507C>A	NCBI36
NG_011591.1:g.134983C>A , LRG_230:g.134983C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000091.5:c.3395C>A (COL4A3) MANE Select	NP_000082.2:p.Pro1132His
ENST00000396578.8:c.3395C>A (COL4A3) MANE Select	ENSP00000379823.3:p.Pro1132His
NM_000091.4:c.3395C>A , LRG_230t1:c.3395C>A (COL4A3)	NP_000082.2:p.Pro1132His
NR_102371.1:n.243+10913G>T (MFF-DT)
ENST00000396578.7:c.3395C>A (COL4A3)	ENSP00000379823.3:p.Pro1132His
XM_005246276.2:c.3395C>A (COL4A3)	XP_005246333.1:p.Pro1132His
XM_005246277.2:c.3290C>A (COL4A3)	XP_005246334.1:p.Pro1097His
XM_005246277.3:c.3290C>A (COL4A3)	XP_005246334.1:p.Pro1097His
XM_006712245.2:c.3395C>A (COL4A3)	XP_006712308.1:p.Pro1132His
XM_006712245.3:c.3395C>A (COL4A3)	XP_006712308.1:p.Pro1132His
XM_011510555.1:c.3395C>A (COL4A3)	XP_011508857.1:p.Pro1132His
XM_011510556.1:c.2156C>A (COL4A3)	XP_011508858.1:p.Pro719His
XM_011510556.2:c.2156C>A (COL4A3)	XP_011508858.1:p.Pro719His
XR_001738601.1:n.3533C>A (COL4A3)
XR_241280.2:n.3533C>A (COL4A3)
XR_241280.3:n.3533C>A (COL4A3)