Canonical Allele Identifier: CA1363079431
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48570204A= , CM000665.2:g.48570204A= GRCh38
NC_000003.11:g.48607637A= , CM000665.1:g.48607637A= GRCh37
NC_000003.10:g.48582641A= NCBI36
NG_007065.1:g.30049T= , LRG_286:g.30049T=

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.7441-26T= MANE Select ENSP00000506558.1:n.7441-26T=
ENST00000328333.12:c.7441-26T= ENSP00000332371.8:n.7441-26T=
ENST00000422991.1:c.436-26T= ENSP00000391608.1:n.436-26T=
ENST00000459756.5:n.238T=
ENST00000467985.1:n.261T=
ENST00000487017.5:n.4080-26T=
NM_000094.3:c.7441-26T= , LRG_286t1:c.7441-26T= NP_000085.1:n.7441-26T=
XM_011533336.1:c.7468-26T= XP_011531638.1:n.7468-26T=
XM_011533337.1:c.7441-26T= XP_011531639.1:n.7441-26T=
XM_011533338.1:c.7408-26T= XP_011531640.1:n.7408-26T=
XM_011533339.1:c.7468-26T= XP_011531641.1:n.7468-26T=
XM_011533340.1:c.*16T= XP_011531642.1:n.*16T=
XM_011533341.1:c.*2T= XP_011531643.1:n.*2T=
XM_011533342.1:c.7382-26T= XP_011531644.1:n.7382-26T=
XR_940369.1:n.7504-26T=
XR_940370.1:n.7504-26T=
XR_940371.1:n.7504-26T=
XR_940372.1:n.7478-26T=
XM_017005688.1:c.7381-26T= XP_016861177.1:n.7381-26T=
XM_017005689.1:c.7441-26T= XP_016861178.1:n.7441-26T=
XM_017005690.1:c.*16T= XP_016861179.1:n.*16T=
XM_017005691.1:c.*2T= XP_016861180.1:n.*2T=
XM_017005692.1:c.7355-26T= XP_016861181.1:n.7355-26T=
XR_001740003.1:n.7477-26T=
XR_001740004.1:n.7477-26T=
XR_001740005.1:n.7477-26T=
XR_001740006.1:n.7451-26T=
NM_000094.4:c.7441-26T= MANE Select NP_000085.1:n.7441-26T=