Canonical Allele Identifier: CA2378221

Gene: COL7A1

Linked Data

• ClinVar Variation Id: 2917905
• ClinVar RCV Id: RCV003737881
• dbSNP Id: rs774359076
• ExAC: 3:48605128 C / T
• gnomAD v2: 3-48605128-C-T
• gnomAD v3: 3-48567695-C-T
• gnomAD v4: 3-48567695-C-T
• MyVariant Identifiers: chr3:g.48605128C>T (hg19) ; chr3:g.48567695C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48567695C>T , CM000665.2:g.48567695C>T	GRCh38
NC_000003.11:g.48605128C>T , CM000665.1:g.48605128C>T	GRCh37
NC_000003.10:g.48580132C>T	NCBI36
NG_007065.1:g.32558G>A , LRG_286:g.32558G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7983+15G>A MANE Select	ENSP00000506558.1:n.7983+15G>A
ENST00000328333.12:c.7983+15G>A	ENSP00000332371.8:n.7983+15G>A
ENST00000487017.5:n.4622+15G>A
NM_000094.3:c.7983+15G>A , LRG_286t1:c.7983+15G>A	NP_000085.1:n.7983+15G>A
XM_011533336.1:c.8010+15G>A	XP_011531638.1:n.8010+15G>A
XM_011533337.1:c.7983+15G>A	XP_011531639.1:n.7983+15G>A
XM_011533338.1:c.7950+15G>A	XP_011531640.1:n.7950+15G>A
XR_940369.1:n.8046+15G>A
XR_940370.1:n.8046+15G>A
XR_940371.1:n.8046+15G>A
XM_017005688.1:c.7923+15G>A	XP_016861177.1:n.7923+15G>A
XR_001740003.1:n.8019+15G>A
XR_001740004.1:n.8019+15G>A
XR_001740005.1:n.8019+15G>A
NM_000094.4:c.7983+15G>A MANE Select	NP_000085.1:n.7983+15G>A