Canonical Allele Identifier: CA907758805

Gene: COL7A1

Linked Data

• dbSNP Id: rs1443388798
• gnomAD v3: 3-48570237-G-C
• gnomAD v4: 3-48570237-G-C
• MyVariant Identifiers: chr3:g.48607670G>C (hg19) ; chr3:g.48570237G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48570237G>C , CM000665.2:g.48570237G>C	GRCh38
NC_000003.11:g.48607670G>C , CM000665.1:g.48607670G>C	GRCh37
NC_000003.10:g.48582674G>C	NCBI36
NG_007065.1:g.30016C>G , LRG_286:g.30016C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7440+38C>G MANE Select	ENSP00000506558.1:n.7440+38C>G
ENST00000328333.12:c.7440+38C>G	ENSP00000332371.8:n.7440+38C>G
ENST00000422991.1:c.435+38C>G	ENSP00000391608.1:n.435+38C>G
ENST00000459756.5:n.205C>G
ENST00000467985.1:n.228C>G
ENST00000487017.5:n.4079+38C>G
NM_000094.3:c.7440+38C>G , LRG_286t1:c.7440+38C>G	NP_000085.1:n.7440+38C>G
XM_011533336.1:c.7467+38C>G	XP_011531638.1:n.7467+38C>G
XM_011533337.1:c.7440+38C>G	XP_011531639.1:n.7440+38C>G
XM_011533338.1:c.7408-59C>G	XP_011531640.1:n.7408-59C>G
XM_011533339.1:c.7467+38C>G	XP_011531641.1:n.7467+38C>G
XM_011533340.1:c.7423C>G	XP_011531642.1:p.Pro2475Ala
XM_011533341.1:c.7397C>G	XP_011531643.1:p.Ser2466Cys
XM_011533342.1:c.7382-59C>G	XP_011531644.1:n.7382-59C>G
XR_940369.1:n.7503+38C>G
XR_940370.1:n.7503+38C>G
XR_940371.1:n.7503+38C>G
XR_940372.1:n.7477+38C>G
XM_017005688.1:c.7381-59C>G	XP_016861177.1:n.7381-59C>G
XM_017005689.1:c.7440+38C>G	XP_016861178.1:n.7440+38C>G
XM_017005690.1:c.7396C>G	XP_016861179.1:p.Pro2466Ala
XM_017005691.1:c.7370C>G	XP_016861180.1:p.Ser2457Cys
XM_017005692.1:c.7355-59C>G	XP_016861181.1:n.7355-59C>G
XR_001740003.1:n.7476+38C>G
XR_001740004.1:n.7476+38C>G
XR_001740005.1:n.7476+38C>G
XR_001740006.1:n.7450+38C>G
NM_000094.4:c.7440+38C>G MANE Select	NP_000085.1:n.7440+38C>G