Canonical Allele Identifier: CA2739279097
Gene: COL7A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2782167
ClinVar RCV Id: RCV003663788

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48575407_48575415dup , CM000665.2:g.48575407_48575415dup GRCh38
NC_000003.11:g.48612840_48612848dup , CM000665.1:g.48612840_48612848dup GRCh37
NC_000003.10:g.48587844_48587852dup NCBI36
NG_007065.1:g.24845_24853dup , LRG_286:g.24845_24853dup

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.6111_6119dup MANE Select ENSP00000506558.1:p.Gly2040_Ile2041insLys...
ENST00000328333.12:c.6111_6119dup ENSP00000332371.8:p.Gly2040_Ile2041insLys...
ENST00000487017.5:n.2028_2036dup
NM_000094.3:c.6111_6119dup , LRG_286t1:c.6111_6119dup NP_000085.1:p.Gly2040_Ile2041insLysProGly...
XM_011533336.1:c.6138_6146dup XP_011531638.1:p.Gly2049_Ile2050insLysPro...
XM_011533337.1:c.6111_6119dup XP_011531639.1:p.Gly2040_Ile2041insLysPro...
XM_011533338.1:c.6138_6146dup XP_011531640.1:p.Gly2049_Ile2050insLysPro...
XM_011533339.1:c.6138_6146dup XP_011531641.1:p.Gly2049_Ile2050insLysPro...
XM_011533340.1:c.6138_6146dup XP_011531642.1:p.Gly2049_Ile2050insLysPro...
XM_011533341.1:c.6138_6146dup XP_011531643.1:p.Gly2049_Ile2050insLysPro...
XM_011533342.1:c.6138_6146dup XP_011531644.1:p.Gly2049_Ile2050insLysPro...
XR_940369.1:n.6174_6182dup
XR_940370.1:n.6174_6182dup
XR_940371.1:n.6174_6182dup
XR_940372.1:n.6174_6182dup
XR_940373.1:n.6174_6182dup
XR_940374.1:n.6174_6182dup
XR_940375.1:n.6174_6181+1dup
XM_017005688.1:c.6111_6119dup XP_016861177.1:p.Gly2040_Ile2041insLysPro...
XM_017005689.1:c.6111_6119dup XP_016861178.1:p.Gly2040_Ile2041insLysPro...
XM_017005690.1:c.6111_6119dup XP_016861179.1:p.Gly2040_Ile2041insLysPro...
XM_017005691.1:c.6111_6119dup XP_016861180.1:p.Gly2040_Ile2041insLysPro...
XM_017005692.1:c.6111_6119dup XP_016861181.1:p.Gly2040_Ile2041insLysPro...
XR_001740003.1:n.6147_6155dup
XR_001740004.1:n.6147_6155dup
XR_001740005.1:n.6147_6155dup
XR_001740006.1:n.6147_6155dup
XR_001740007.1:n.6147_6155dup
XR_001740008.1:n.6147_6155dup
XR_001740009.1:n.6147_6154+1dup
NM_000094.4:c.6111_6119dup MANE Select NP_000085.1:p.Gly2040_Ile2041insLysProGly...