Canonical Allele Identifier: CA410521927
Gene: COL6A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.46112393C>A , CM000683.2:g.46112393C>A GRCh38
NC_000021.8:g.47532307C>A , CM000683.1:g.47532307C>A GRCh37
NC_000021.7:g.46356735C>A NCBI36
NG_008675.1:g.19275C>A , LRG_476:g.19275C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000397763.6:c.530C>A MANE Plus Clinical ENSP00000380870.1:p.Ala177Asp
ENST00000300527.9:c.530C>A MANE Select ENSP00000300527.4:p.Ala177Asp
ENST00000409416.6:c.530C>A ENSP00000387115.1:p.Ala177Asp
ENST00000300527.8:c.530C>A ENSP00000300527.4:p.Ala177Asp
ENST00000310645.9:c.530C>A ENSP00000312529.5:p.Ala177Asp
ENST00000397763.5:c.530C>A ENSP00000380870.1:p.Ala177Asp
ENST00000409416.5:c.530C>A ENSP00000387115.1:p.Ala177Asp
ENST00000436769.5:c.530C>A ENSP00000390418.1:p.Ala177Asp
NM_001849.3:c.530C>A , LRG_476t1:c.530C>A NP_001840.3:p.Ala177Asp
NM_058174.2:c.530C>A NP_478054.2:p.Ala177Asp
NM_058175.2:c.530C>A NP_478055.2:p.Ala177Asp
XM_011529451.1:c.530C>A XP_011527753.1:p.Ala177Asp
XM_011529452.1:c.530C>A XP_011527754.1:p.Ala177Asp
XR_937438.1:n.653C>A
XR_937439.1:n.653C>A
XR_937438.2:n.660C>A
XR_937439.2:n.660C>A
NM_001849.4:c.530C>A MANE Select NP_001840.3:p.Ala177Asp
NM_058174.3:c.530C>A MANE Plus Clinical NP_478054.2:p.Ala177Asp
NM_058175.3:c.530C>A NP_478055.2:p.Ala177Asp