Canonical Allele Identifier: CA2654968396
Gene: COL6A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46113743_46113746dup , CM000683.2:g.46113743_46113746dup GRCh38
NC_000021.8:g.47533657_47533660dup , CM000683.1:g.47533657_47533660dup GRCh37
NC_000021.7:g.46358085_46358088dup NCBI36
NG_008675.1:g.20625_20628dup , LRG_476:g.20625_20628dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000397763.6:c.736-265_736-262dup MANE Plus Clinical ENSP00000380870.1:n.736-265_736-262dup
ENST00000300527.9:c.736-265_736-262dup MANE Select ENSP00000300527.4:n.736-265_736-262dup
ENST00000409416.6:c.736-265_736-262dup ENSP00000387115.1:n.736-265_736-262dup
ENST00000300527.8:c.736-265_736-262dup ENSP00000300527.4:n.736-265_736-262dup
ENST00000310645.9:c.736-265_736-262dup ENSP00000312529.5:n.736-265_736-262dup
ENST00000397763.5:c.736-265_736-262dup ENSP00000380870.1:n.736-265_736-262dup
ENST00000409416.5:c.736-265_736-262dup ENSP00000387115.1:n.736-265_736-262dup
ENST00000485591.1:n.127_130dup
NM_001849.3:c.736-265_736-262dup , LRG_476t1:c.736-265_736-262dup NP_001840.3:n.736-265_736-262dup
NM_058174.2:c.736-265_736-262dup NP_478054.2:n.736-265_736-262dup
NM_058175.2:c.736-265_736-262dup NP_478055.2:n.736-265_736-262dup
XM_011529451.1:c.736-265_736-262dup XP_011527753.1:n.736-265_736-262dup
XM_011529452.1:c.736-265_736-262dup XP_011527754.1:n.736-265_736-262dup
XR_937438.1:n.859-265_859-262dup
XR_937439.1:n.859-265_859-262dup
XR_937438.2:n.866-265_866-262dup
XR_937439.2:n.866-265_866-262dup
NM_001849.4:c.736-265_736-262dup MANE Select NP_001840.3:n.736-265_736-262dup
NM_058174.3:c.736-265_736-262dup MANE Plus Clinical NP_478054.2:n.736-265_736-262dup
NM_058175.3:c.736-265_736-262dup NP_478055.2:n.736-265_736-262dup