Canonical Allele Identifier: CA2392507581
Gene: COL6A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46125812_46125835delinsGCCACGAGGGCACCTTTGAGGCCA , CM000683.2:g.46125812_46125835delinsGCCACGAGGGCACCTTTGAGGCCA GRCh38
NC_000021.8:g.47545726_47545749delinsGCCACGAGGGCACCTTTGAGGCCA , CM000683.1:g.47545726_47545749delinsGCCACGAGGGCACCTTTGAGGCCA GRCh37
NC_000021.7:g.46370154_46370177delinsGCCACGAGGGCACCTTTGAGGCCA NCBI36
NG_008675.1:g.32694_32717delinsGCCACGAGGGCACCTTTGAGGCCA , LRG_476:g.32694_32717delinsGCCACGAGGGCACCTTTGAGGCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000397763.6:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA MANE Plus Clinical ENSP00000380870.1:p.Ser666=
ENST00000300527.9:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA MANE Select ENSP00000300527.4:p.Ser666=
ENST00000409416.6:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA ENSP00000387115.1:p.Ser666=
ENST00000300527.8:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA ENSP00000300527.4:p.Ser666=
ENST00000310645.9:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA ENSP00000312529.5:p.Ser666=
ENST00000397763.5:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA ENSP00000380870.1:p.Ser666=
ENST00000409416.5:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA ENSP00000387115.1:p.Ser666=
ENST00000413758.1:c.668_691delinsGCCACGAGGGCACCTTTGAGGCCA ENSP00000395751.1:p.Ser223=
NM_001849.3:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA , LRG_476t1:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA NP_001840.3:p.Ser666=
NM_058174.2:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA NP_478054.2:p.Ser666=
NM_058175.2:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA NP_478055.2:p.Ser666=
XM_011529451.1:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA XP_011527753.1:p.Ser666=
XM_011529452.1:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA XP_011527754.1:p.Ser666=
XR_937438.1:n.2074_2097delinsGCCACGAGGGCACCTTTGAGGCCA
XR_937439.1:n.2074_2097delinsGCCACGAGGGCACCTTTGAGGCCA
XR_937438.2:n.2081_2104delinsGCCACGAGGGCACCTTTGAGGCCA
XR_937439.2:n.2081_2104delinsGCCACGAGGGCACCTTTGAGGCCA
NM_001849.4:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA MANE Select NP_001840.3:p.Ser666=
NM_058174.3:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA MANE Plus Clinical NP_478054.2:p.Ser666=
NM_058175.3:c.1997_2020delinsGCCACGAGGGCACCTTTGAGGCCA NP_478055.2:p.Ser666=