Canonical Allele Identifier: CA539907266

Gene: COL4A3 MFF-DT

Linked Data

• dbSNP Id: rs1246973381
• gnomAD v2: 2-228176693-T-C
• gnomAD v4: 2-227311977-T-C
• MyVariant Identifiers: chr2:g.228176693T>C (hg19) ; chr2:g.227311977T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227311977T>C , CM000664.2:g.227311977T>C	GRCh38
NC_000002.11:g.228176693T>C , CM000664.1:g.228176693T>C	GRCh37
NC_000002.10:g.227884937T>C	NCBI36
NG_011591.1:g.152413T>C , LRG_230:g.152413T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471862.2:n.2378T>C (COL4A3)
ENST00000682257.1:n.342T>C (COL4A3)
ENST00000682970.1:n.418T>C (COL4A3)
ENST00000683077.1:n.2059T>C (COL4A3)
ENST00000684413.1:n.2687T>C (COL4A3)
ENST00000684724.1:n.541T>C (COL4A3)
ENST00000396578.8:c.*107T>C (COL4A3) MANE Select	ENSP00000379823.3:n.*107T>C
ENST00000396578.7:c.*107T>C (COL4A3)	ENSP00000379823.3:n.*107T>C
NM_000091.4:c.*107T>C , LRG_230t1:c.*107T>C (COL4A3)	NP_000082.2:n.*107T>C
NR_102371.1:n.48-6322A>G (MFF-DT)
XM_005246276.2:c.*33T>C (COL4A3)	XP_005246333.1:n.*33T>C
XM_005246277.2:c.*107T>C (COL4A3)	XP_005246334.1:n.*107T>C
XM_011510556.1:c.*107T>C (COL4A3)	XP_011508858.1:n.*107T>C
XR_241280.2:n.5080T>C (COL4A3)
XM_005246277.3:c.*107T>C (COL4A3)	XP_005246334.1:n.*107T>C
XM_011510556.2:c.*107T>C (COL4A3)	XP_011508858.1:n.*107T>C
XR_241280.3:n.5080T>C (COL4A3)
NM_000091.5:c.*107T>C (COL4A3) MANE Select	NP_000082.2:n.*107T>C