Canonical Allele Identifier: CA410521927

Gene: COL6A2

Linked Data

• gnomAD v4: 21-46112393-C-A
• MyVariant Identifiers: chr21:g.47532307C>A (hg19) ; chr21:g.46112393C>A (hg38)

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