Canonical Allele Identifier: CA1363079026
Gene: COL7A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48565466G= , CM000665.2:g.48565466G= GRCh38
NC_000003.11:g.48602899G= , CM000665.1:g.48602899G= GRCh37
NC_000003.10:g.48577903G= NCBI36
NG_007065.1:g.34787C= , LRG_286:g.34787C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681320.1:c.8471C= MANE Select ENSP00000506558.1:p.Ala2824=
ENST00000328333.12:c.8471C= ENSP00000332371.8:p.Ala2824=
ENST00000487017.5:n.5110C=
NM_000094.3:c.8471C= , LRG_286t1:c.8471C= NP_000085.1:p.Ala2824=
XM_011533336.1:c.8498C= XP_011531638.1:p.Ala2833=
XM_011533337.1:c.8471C= XP_011531639.1:p.Ala2824=
XM_011533338.1:c.8438C= XP_011531640.1:p.Ala2813=
XR_940369.1:n.8534C=
XR_940370.1:n.8534C=
XR_940371.1:n.8534C=
XM_017005688.1:c.8411C= XP_016861177.1:p.Ala2804=
XR_001740003.1:n.8507C=
XR_001740004.1:n.8507C=
XR_001740005.1:n.8507C=
NM_000094.4:c.8471C= MANE Select NP_000085.1:p.Ala2824=