Canonical Allele Identifier: CA350861838

Gene: COL4A3 MFF-DT

Linked Data

• MyVariant Identifiers: chr2:g.228111443C>G (hg19) ; chr2:g.227246727C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227246727C>G , CM000664.2:g.227246727C>G	GRCh38
NC_000002.11:g.228111443C>G , CM000664.1:g.228111443C>G	GRCh37
NC_000002.10:g.227819687C>G	NCBI36
NG_011591.1:g.87163C>G , LRG_230:g.87163C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396578.8:c.430C>G (COL4A3) MANE Select	ENSP00000379823.3:p.Pro144Ala
ENST00000396578.7:c.430C>G (COL4A3)	ENSP00000379823.3:p.Pro144Ala
NM_000091.4:c.430C>G , LRG_230t1:c.430C>G (COL4A3)	NP_000082.2:p.Pro144Ala
NR_102371.1:n.1593-8553G>C (MFF-DT)
XM_005246276.2:c.430C>G (COL4A3)	XP_005246333.1:p.Pro144Ala
XM_005246277.2:c.430C>G (COL4A3)	XP_005246334.1:p.Pro144Ala
XM_005246280.2:c.430C>G (COL4A3)	XP_005246337.1:p.Pro144Ala
XM_006712245.2:c.430C>G (COL4A3)	XP_006712308.1:p.Pro144Ala
XM_011510555.1:c.430C>G (COL4A3)	XP_011508857.1:p.Pro144Ala
XR_241280.2:n.568C>G (COL4A3)
XM_005246277.3:c.430C>G (COL4A3)	XP_005246334.1:p.Pro144Ala
XM_005246280.3:c.430C>G (COL4A3)	XP_005246337.1:p.Pro144Ala
XM_006712245.3:c.430C>G (COL4A3)	XP_006712308.1:p.Pro144Ala
XM_017003295.1:c.430C>G (COL4A3)	XP_016858784.1:p.Pro144Ala
XR_001738601.1:n.568C>G (COL4A3)
XR_241280.3:n.568C>G (COL4A3)
NM_000091.5:c.430C>G (COL4A3) MANE Select	NP_000082.2:p.Pro144Ala