Canonical Allele Identifier: CA352646410
Gene: COL7A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48570313G>C , CM000665.2:g.48570313G>C GRCh38
NC_000003.11:g.48607746G>C , CM000665.1:g.48607746G>C GRCh37
NC_000003.10:g.48582750G>C NCBI36
NG_007065.1:g.29940C>G , LRG_286:g.29940C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.7402C>G MANE Select ENSP00000506558.1:p.Pro2468Ala
ENST00000328333.12:c.7402C>G ENSP00000332371.8:p.Pro2468Ala
ENST00000422991.1:c.397C>G ENSP00000391608.1:p.Pro133Ala
ENST00000459756.5:n.129C>G
ENST00000467985.1:n.152C>G
ENST00000487017.5:n.4041C>G
NM_000094.3:c.7402C>G , LRG_286t1:c.7402C>G NP_000085.1:p.Pro2468Ala
XM_011533336.1:c.7429C>G XP_011531638.1:p.Pro2477Ala
XM_011533337.1:c.7402C>G XP_011531639.1:p.Pro2468Ala
XM_011533338.1:c.7408-135C>G XP_011531640.1:p.=
XM_011533339.1:c.7429C>G XP_011531641.1:p.Pro2477Ala
XM_011533340.1:c.7408-61C>G XP_011531642.1:p.=
XM_011533341.1:c.7382-61C>G XP_011531643.1:p.=
XM_011533342.1:c.7382-135C>G XP_011531644.1:p.=
XR_940369.1:n.7465C>G
XR_940370.1:n.7465C>G
XR_940371.1:n.7465C>G
XR_940372.1:n.7439C>G
XM_017005688.1:c.7381-135C>G XP_016861177.1:p.=
XM_017005689.1:c.7402C>G XP_016861178.1:p.Pro2468Ala
XM_017005690.1:c.7381-61C>G XP_016861179.1:p.=
XM_017005691.1:c.7355-61C>G XP_016861180.1:p.=
XM_017005692.1:c.7355-135C>G XP_016861181.1:p.=
XR_001740003.1:n.7438C>G
XR_001740004.1:n.7438C>G
XR_001740005.1:n.7438C>G
XR_001740006.1:n.7412C>G
NM_000094.4:c.7402C>G MANE Select NP_000085.1:p.Pro2468Ala