Canonical Allele Identifier: CA10070711

Gene: COL6A1

Linked Data

• ClinVar Variation Id: 340326
• ClinVar RCV Id: RCV000262534 ; RCV000734301 ; RCV001089264
• dbSNP Id: rs370780432
• ExAC: 21:47421898 G / A
• gnomAD v2: 21-47421898-G-A
• gnomAD v3: 21-46001984-G-A
• gnomAD v4: 21-46001984-G-A
• COSMIC: COSM579391
• MyVariant Identifiers: chr21:g.47421898G>A (hg19) ; chr21:g.46001984G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46001984G>A , CM000683.2:g.46001984G>A	GRCh38
NC_000021.8:g.47421898G>A , CM000683.1:g.47421898G>A	GRCh37
NC_000021.7:g.46246326G>A	NCBI36
NG_008674.1:g.25236G>A , LRG_475:g.25236G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463060.6:n.379G>A
ENST00000612273.2:c.106G>A
ENST00000682634.1:c.106G>A
ENST00000361866.8:c.1980G>A MANE Select	ENSP00000355180.3:p.Ala660=
ENST00000361866.7:c.1980G>A	ENSP00000355180.3:p.Ala660=
ENST00000463060.5:n.379G>A
ENST00000498614.5:n.214G>A
ENST00000612273.1:c.1974G>A	ENSP00000483630.1:p.Ala658=
NM_001848.2:c.1980G>A , LRG_475t1:c.1980G>A	NP_001839.2:p.Ala660=
NM_001848.3:c.1980G>A MANE Select	NP_001839.2:p.Ala660=