Canonical Allele Identifier: CA352673538

Gene: COL7A1 MIR711

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48578929G>A , CM000665.2:g.48578929G>A	GRCh38
NC_000003.11:g.48616362G>A , CM000665.1:g.48616362G>A	GRCh37
NC_000003.10:g.48591366G>A	NCBI36
NG_007065.1:g.21324C>T , LRG_286:g.21324C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.5414C>T (COL7A1) MANE Select	ENSP00000506558.1:p.Pro1805Leu
ENST00000328333.12:c.5414C>T (COL7A1)	ENSP00000332371.8:p.Pro1805Leu
ENST00000487017.5:n.1331C>T (COL7A1)
NM_000094.3:c.5414C>T , LRG_286t1:c.5414C>T (COL7A1)	NP_000085.1:p.Pro1805Leu
NR_031756.1:n.49C>T (MIR711)
XM_011533336.1:c.5441C>T (COL7A1)	XP_011531638.1:p.Pro1814Leu
XM_011533337.1:c.5414C>T (COL7A1)	XP_011531639.1:p.Pro1805Leu
XM_011533338.1:c.5441C>T (COL7A1)	XP_011531640.1:p.Pro1814Leu
XM_011533339.1:c.5441C>T (COL7A1)	XP_011531641.1:p.Pro1814Leu
XM_011533340.1:c.5441C>T (COL7A1)	XP_011531642.1:p.Pro1814Leu
XM_011533341.1:c.5441C>T (COL7A1)	XP_011531643.1:p.Pro1814Leu
XM_011533342.1:c.5441C>T (COL7A1)	XP_011531644.1:p.Pro1814Leu
XR_940369.1:n.5477C>T (COL7A1)
XR_940370.1:n.5477C>T (COL7A1)
XR_940371.1:n.5477C>T (COL7A1)
XR_940372.1:n.5477C>T (COL7A1)
XR_940373.1:n.5477C>T (COL7A1)
XR_940374.1:n.5477C>T (COL7A1)
XR_940375.1:n.5477C>T (COL7A1)
XM_017005688.1:c.5414C>T (COL7A1)	XP_016861177.1:p.Pro1805Leu
XM_017005689.1:c.5414C>T (COL7A1)	XP_016861178.1:p.Pro1805Leu
XM_017005690.1:c.5414C>T (COL7A1)	XP_016861179.1:p.Pro1805Leu
XM_017005691.1:c.5414C>T (COL7A1)	XP_016861180.1:p.Pro1805Leu
XM_017005692.1:c.5414C>T (COL7A1)	XP_016861181.1:p.Pro1805Leu
XR_001740003.1:n.5450C>T (COL7A1)
XR_001740004.1:n.5450C>T (COL7A1)
XR_001740005.1:n.5450C>T (COL7A1)
XR_001740006.1:n.5450C>T (COL7A1)
XR_001740007.1:n.5450C>T (COL7A1)
XR_001740008.1:n.5450C>T (COL7A1)
XR_001740009.1:n.5450C>T (COL7A1)
NM_000094.4:c.5414C>T (COL7A1) MANE Select	NP_000085.1:p.Pro1805Leu