Canonical Allele Identifier: CA352642167

Gene: COL7A1

Linked Data

• dbSNP Id: rs1317544123
• gnomAD v2: 3-48605937-C-T
• MyVariant Identifiers: chr3:g.48605937C>T (hg19) ; chr3:g.48568504C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48568504C>T , CM000665.2:g.48568504C>T	GRCh38
NC_000003.11:g.48605937C>T , CM000665.1:g.48605937C>T	GRCh37
NC_000003.10:g.48580941C>T	NCBI36
NG_007065.1:g.31749G>A , LRG_286:g.31749G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.7789G>A MANE Select	ENSP00000506558.1:p.Asp2597Asn
ENST00000328333.12:c.7789G>A	ENSP00000332371.8:p.Asp2597Asn
ENST00000459756.5:n.612G>A
ENST00000467985.1:n.635G>A
ENST00000487017.5:n.4428G>A
NM_000094.3:c.7789G>A , LRG_286t1:c.7789G>A	NP_000085.1:p.Asp2597Asn
XM_011533336.1:c.7816G>A	XP_011531638.1:p.Asp2606Asn
XM_011533337.1:c.7789G>A	XP_011531639.1:p.Asp2597Asn
XM_011533338.1:c.7756G>A	XP_011531640.1:p.Asp2586Asn
XM_011533339.1:c.7816G>A	XP_011531641.1:p.Asp2606Asn
XR_940369.1:n.7852G>A
XR_940370.1:n.7852G>A
XR_940371.1:n.7852G>A
XR_940372.1:n.7826G>A
XM_017005688.1:c.7729G>A	XP_016861177.1:p.Asp2577Asn
XM_017005689.1:c.7789G>A	XP_016861178.1:p.Asp2597Asn
XR_001740003.1:n.7825G>A
XR_001740004.1:n.7825G>A
XR_001740005.1:n.7825G>A
XR_001740006.1:n.7799G>A
NM_000094.4:c.7789G>A MANE Select	NP_000085.1:p.Asp2597Asn