Canonical Allele Identifier: CA433533966
Gene: COL7A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.48607738G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48570305G>A , CM000665.2:g.48570305G>A GRCh38
NC_000003.11:g.48607738G>A , CM000665.1:g.48607738G>A GRCh37
NC_000003.10:g.48582742G>A NCBI36
NG_007065.1:g.29948C>T , LRG_286:g.29948C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000681320.1:c.7410C>T MANE Select ENSP00000506558.1:p.Pro2470=
ENST00000328333.12:c.7410C>T ENSP00000332371.8:p.Pro2470=
ENST00000422991.1:c.405C>T ENSP00000391608.1:p.Pro135=
ENST00000459756.5:n.137C>T
ENST00000467985.1:n.160C>T
ENST00000487017.5:n.4049C>T
NM_000094.3:c.7410C>T , LRG_286t1:c.7410C>T NP_000085.1:p.Pro2470=
XM_011533336.1:c.7437C>T XP_011531638.1:p.Pro2479=
XM_011533337.1:c.7410C>T XP_011531639.1:p.Pro2470=
XM_011533338.1:c.7408-127C>T XP_011531640.1:p.=
XM_011533339.1:c.7437C>T XP_011531641.1:p.Pro2479=
XM_011533340.1:c.7408-53C>T XP_011531642.1:p.=
XM_011533341.1:c.7382-53C>T XP_011531643.1:p.=
XM_011533342.1:c.7382-127C>T XP_011531644.1:p.=
XR_940369.1:n.7473C>T
XR_940370.1:n.7473C>T
XR_940371.1:n.7473C>T
XR_940372.1:n.7447C>T
XM_017005688.1:c.7381-127C>T XP_016861177.1:p.=
XM_017005689.1:c.7410C>T XP_016861178.1:p.Pro2470=
XM_017005690.1:c.7381-53C>T XP_016861179.1:p.=
XM_017005691.1:c.7355-53C>T XP_016861180.1:p.=
XM_017005692.1:c.7355-127C>T XP_016861181.1:p.=
XR_001740003.1:n.7446C>T
XR_001740004.1:n.7446C>T
XR_001740005.1:n.7446C>T
XR_001740006.1:n.7420C>T
NM_000094.4:c.7410C>T MANE Select NP_000085.1:p.Pro2470=