Canonical Allele Identifier: CA2818100860

Gene: COL6A2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46113599_46113607del , CM000683.2:g.46113599_46113607del	GRCh38
NC_000021.8:g.47533513_47533521del , CM000683.1:g.47533513_47533521del	GRCh37
NC_000021.7:g.46357941_46357949del	NCBI36
NG_008675.1:g.20481_20489del , LRG_476:g.20481_20489del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397763.6:c.736-409_736-401del MANE Plus Clinical	ENSP00000380870.1:n.736-409_736-401del
ENST00000300527.9:c.736-409_736-401del MANE Select	ENSP00000300527.4:n.736-409_736-401del
ENST00000409416.6:c.736-409_736-401del	ENSP00000387115.1:n.736-409_736-401del
ENST00000300527.8:c.736-409_736-401del	ENSP00000300527.4:n.736-409_736-401del
ENST00000310645.9:c.736-409_736-401del	ENSP00000312529.5:n.736-409_736-401del
ENST00000397763.5:c.736-409_736-401del	ENSP00000380870.1:n.736-409_736-401del
ENST00000409416.5:c.736-409_736-401del	ENSP00000387115.1:n.736-409_736-401del
NM_001849.3:c.736-409_736-401del , LRG_476t1:c.736-409_736-401del	NP_001840.3:n.736-409_736-401del
NM_058174.2:c.736-409_736-401del	NP_478054.2:n.736-409_736-401del
NM_058175.2:c.736-409_736-401del	NP_478055.2:n.736-409_736-401del
XM_011529451.1:c.736-409_736-401del	XP_011527753.1:n.736-409_736-401del
XM_011529452.1:c.736-409_736-401del	XP_011527754.1:n.736-409_736-401del
XR_937438.1:n.859-409_859-401del
XR_937439.1:n.859-409_859-401del
XR_937438.2:n.866-409_866-401del
XR_937439.2:n.866-409_866-401del
NM_001849.4:c.736-409_736-401del MANE Select	NP_001840.3:n.736-409_736-401del
NM_058174.3:c.736-409_736-401del MANE Plus Clinical	NP_478054.2:n.736-409_736-401del
NM_058175.3:c.736-409_736-401del	NP_478055.2:n.736-409_736-401del