Canonical Allele Identifier: CA351188006

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238243287G>T (hg19) ; chr2:g.237334644G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237334644G>T , CM000664.2:g.237334644G>T	GRCh38
NC_000002.11:g.238243287G>T , CM000664.1:g.238243287G>T	GRCh37
NC_000002.10:g.237908026G>T	NCBI36
NG_008676.1:g.84564C>A , LRG_473:g.84564C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1611-1096C>A
ENST00000353578.9:c.8593C>A	ENSP00000315873.4:p.His2865Asn
ENST00000682957.1:c.1338C>A
ENST00000683348.1:c.79C>A	ENSP00000508058.1:p.His27Asn
ENST00000295550.9:c.9211C>A MANE Select	ENSP00000295550.4:p.His3071Asn
ENST00000295550.8:c.9211C>A	ENSP00000295550.4:p.His3071Asn
ENST00000347401.7:c.7387C>A	ENSP00000315609.4:p.His2463Asn
ENST00000353578.8:c.8593C>A	ENSP00000315873.4:p.His2865Asn
ENST00000409809.5:c.8593C>A	ENSP00000386844.1:p.His2865Asn
ENST00000472056.5:c.7390C>A	ENSP00000418285.1:p.His2464Asn
ENST00000491769.1:n.5653C>A
ENST00000493608.1:n.143C>A
NM_004369.3:c.9211C>A , LRG_473t1:c.9211C>A	NP_004360.2:p.His3071Asn
NM_057166.4:c.7390C>A	NP_476507.3:p.His2464Asn
NM_057167.3:c.8593C>A	NP_476508.2:p.His2865Asn
XM_005246065.1:c.8611C>A	XP_005246122.1:p.His2871Asn
XM_005246066.1:c.7990C>A	XP_005246123.1:p.His2664Asn
XM_006712253.1:c.8710C>A	XP_006712316.1:p.His2904Asn
XM_011510574.1:c.9208C>A	XP_011508876.1:p.His3070Asn
XM_011510575.1:c.6805C>A	XP_011508877.1:p.His2269Asn
XM_017003304.1:c.6805C>A	XP_016858793.1:p.His2269Asn
XM_024452684.1:c.7990C>A	XP_024308452.1:p.His2664Asn
NM_004369.4:c.9211C>A MANE Select	NP_004360.2:p.His3071Asn
NM_057166.5:c.7390C>A	NP_476507.3:p.His2464Asn
NM_057167.4:c.8593C>A	NP_476508.2:p.His2865Asn