Canonical Allele Identifier: CA351202651

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238253171T>G (hg19) ; chr2:g.237344528T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344528T>G , CM000664.2:g.237344528T>G	GRCh38
NC_000002.11:g.238253171T>G , CM000664.1:g.238253171T>G	GRCh37
NC_000002.10:g.237917910T>G	NCBI36
NG_008676.1:g.74680A>C , LRG_473:g.74680A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.135A>C
ENST00000353578.9:c.6872A>C	ENSP00000315873.4:p.Asn2291Thr
ENST00000295550.9:c.7490A>C MANE Select	ENSP00000295550.4:p.Asn2497Thr
ENST00000295550.8:c.7490A>C	ENSP00000295550.4:p.Asn2497Thr
ENST00000347401.7:c.5666A>C	ENSP00000315609.4:p.Asn1889Thr
ENST00000353578.8:c.6872A>C	ENSP00000315873.4:p.Asn2291Thr
ENST00000409809.5:c.6872A>C	ENSP00000386844.1:p.Asn2291Thr
ENST00000472056.5:c.5669A>C	ENSP00000418285.1:p.Asn1890Thr
ENST00000491769.1:n.1744A>C
NM_004369.3:c.7490A>C , LRG_473t1:c.7490A>C	NP_004360.2:p.Asn2497Thr
NM_057166.4:c.5669A>C	NP_476507.3:p.Asn1890Thr
NM_057167.3:c.6872A>C	NP_476508.2:p.Asn2291Thr
XM_005246065.1:c.6890A>C	XP_005246122.1:p.Asn2297Thr
XM_005246066.1:c.6269A>C	XP_005246123.1:p.Asn2090Thr
XM_006712253.1:c.6989A>C	XP_006712316.1:p.Asn2330Thr
XM_011510574.1:c.7487A>C	XP_011508876.1:p.Asn2496Thr
XM_011510575.1:c.5084A>C	XP_011508877.1:p.Asn1695Thr
XM_017003304.1:c.5084A>C	XP_016858793.1:p.Asn1695Thr
XM_024452684.1:c.6269A>C	XP_024308452.1:p.Asn2090Thr
NM_004369.4:c.7490A>C MANE Select	NP_004360.2:p.Asn2497Thr
NM_057166.5:c.5669A>C	NP_476507.3:p.Asn1890Thr
NM_057167.4:c.6872A>C	NP_476508.2:p.Asn2291Thr