Canonical Allele Identifier: CA2654968214
Gene: COL6A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46113659_46113677dup , CM000683.2:g.46113659_46113677dup GRCh38
NC_000021.8:g.47533573_47533591dup , CM000683.1:g.47533573_47533591dup GRCh37
NC_000021.7:g.46358001_46358019dup NCBI36
NG_008675.1:g.20541_20559dup , LRG_476:g.20541_20559dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000397763.6:c.736-349_736-331dup MANE Plus Clinical ENSP00000380870.1:n.736-349_736-331dup
ENST00000300527.9:c.736-349_736-331dup MANE Select ENSP00000300527.4:n.736-349_736-331dup
ENST00000409416.6:c.736-349_736-331dup ENSP00000387115.1:n.736-349_736-331dup
ENST00000300527.8:c.736-349_736-331dup ENSP00000300527.4:n.736-349_736-331dup
ENST00000310645.9:c.736-349_736-331dup ENSP00000312529.5:n.736-349_736-331dup
ENST00000397763.5:c.736-349_736-331dup ENSP00000380870.1:n.736-349_736-331dup
ENST00000409416.5:c.736-349_736-331dup ENSP00000387115.1:n.736-349_736-331dup
ENST00000485591.1:n.43_61dup
NM_001849.3:c.736-349_736-331dup , LRG_476t1:c.736-349_736-331dup NP_001840.3:n.736-349_736-331dup
NM_058174.2:c.736-349_736-331dup NP_478054.2:n.736-349_736-331dup
NM_058175.2:c.736-349_736-331dup NP_478055.2:n.736-349_736-331dup
XM_011529451.1:c.736-349_736-331dup XP_011527753.1:n.736-349_736-331dup
XM_011529452.1:c.736-349_736-331dup XP_011527754.1:n.736-349_736-331dup
XR_937438.1:n.859-349_859-331dup
XR_937439.1:n.859-349_859-331dup
XR_937438.2:n.866-349_866-331dup
XR_937439.2:n.866-349_866-331dup
NM_001849.4:c.736-349_736-331dup MANE Select NP_001840.3:n.736-349_736-331dup
NM_058174.3:c.736-349_736-331dup MANE Plus Clinical NP_478054.2:n.736-349_736-331dup
NM_058175.3:c.736-349_736-331dup NP_478055.2:n.736-349_736-331dup