Canonical Allele Identifier: CA2665614101

Gene: COL7A1

Linked Data

• dbSNP Id: rs2107657440
• gnomAD v4: 3-48572567-T-TCCGCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48572569_48572570insGCCCCCCCCCC , CM000665.2:g.48572569_48572570insGCCCCCCCCCC	GRCh38
NC_000003.11:g.48610002_48610003insGCCCCCCCCCC , CM000665.1:g.48610002_48610003insGCCCCCCCCCC	GRCh37
NC_000003.10:g.48585006_48585007insGCCCCCCCCCC	NCBI36
NG_007065.1:g.27685_27686insGGGGGGGGCGG , LRG_286:g.27685_27686insGGGGGGGGCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681320.1:c.6901-30_6901-29insGGGGGGGGCGG MANE Select	ENSP00000506558.1:n.6901-30_6901-29insGGGGGGGGCGG
ENST00000328333.12:c.6901-30_6901-29insGGGGGGGGCGG	ENSP00000332371.8:n.6901-30_6901-29insGGGGGGGGCGG
ENST00000487017.5:n.2818-30_2818-29insGGGGGGGGCGG
NM_000094.3:c.6901-30_6901-29insGGGGGGGGCGG , LRG_286t1:c.6901-30_6901-29insGGGGGGGGCGG	NP_000085.1:n.6901-30_6901-29insGGGGGGGGCGG
XM_011533336.1:c.6928-30_6928-29insGGGGGGGGCGG	XP_011531638.1:n.6928-30_6928-29insGGGGGGGGCGG
XM_011533337.1:c.6901-30_6901-29insGGGGGGGGCGG	XP_011531639.1:n.6901-30_6901-29insGGGGGGGGCGG
XM_011533338.1:c.6928-30_6928-29insGGGGGGGGCGG	XP_011531640.1:n.6928-30_6928-29insGGGGGGGGCGG
XM_011533339.1:c.6928-30_6928-29insGGGGGGGGCGG	XP_011531641.1:n.6928-30_6928-29insGGGGGGGGCGG
XM_011533340.1:c.6928-30_6928-29insGGGGGGGGCGG	XP_011531642.1:n.6928-30_6928-29insGGGGGGGGCGG
XM_011533341.1:c.6928-30_6928-29insGGGGGGGGCGG	XP_011531643.1:n.6928-30_6928-29insGGGGGGGGCGG
XM_011533342.1:c.6928-30_6928-29insGGGGGGGGCGG	XP_011531644.1:n.6928-30_6928-29insGGGGGGGGCGG
XR_940369.1:n.6964-30_6964-29insGGGGGGGGCGG
XR_940370.1:n.6964-30_6964-29insGGGGGGGGCGG
XR_940371.1:n.6964-30_6964-29insGGGGGGGGCGG
XR_940372.1:n.6964-30_6964-29insGGGGGGGGCGG
XR_940373.1:n.6964-30_6964-29insGGGGGGGGCGG
XR_940374.1:n.6974-30_6974-29insGGGGGGGGCGG
XM_017005688.1:c.6901-30_6901-29insGGGGGGGGCGG	XP_016861177.1:n.6901-30_6901-29insGGGGGGGGCGG
XM_017005689.1:c.6901-30_6901-29insGGGGGGGGCGG	XP_016861178.1:n.6901-30_6901-29insGGGGGGGGCGG
XM_017005690.1:c.6901-30_6901-29insGGGGGGGGCGG	XP_016861179.1:n.6901-30_6901-29insGGGGGGGGCGG
XM_017005691.1:c.6901-30_6901-29insGGGGGGGGCGG	XP_016861180.1:n.6901-30_6901-29insGGGGGGGGCGG
XM_017005692.1:c.6901-30_6901-29insGGGGGGGGCGG	XP_016861181.1:n.6901-30_6901-29insGGGGGGGGCGG
XR_001740003.1:n.6937-30_6937-29insGGGGGGGGCGG
XR_001740004.1:n.6937-30_6937-29insGGGGGGGGCGG
XR_001740005.1:n.6937-30_6937-29insGGGGGGGGCGG
XR_001740006.1:n.6937-30_6937-29insGGGGGGGGCGG
XR_001740007.1:n.6937-30_6937-29insGGGGGGGGCGG
XR_001740008.1:n.6947-30_6947-29insGGGGGGGGCGG
NM_000094.4:c.6901-30_6901-29insGGGGGGGGCGG MANE Select	NP_000085.1:n.6901-30_6901-29insGGGGGGGGCGG