Canonical Allele Identifier: CA351192075

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238245174T>A (hg19) ; chr2:g.237336531T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336531T>A , CM000664.2:g.237336531T>A	GRCh38
NC_000002.11:g.238245174T>A , CM000664.1:g.238245174T>A	GRCh37
NC_000002.10:g.237909913T>A	NCBI36
NG_008676.1:g.82677A>T , LRG_473:g.82677A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1214A>T
ENST00000353578.9:c.7951A>T	ENSP00000315873.4:p.Asn2651Tyr
ENST00000682957.1:c.696A>T
ENST00000684508.1:n.836A>T
ENST00000295550.9:c.8569A>T MANE Select	ENSP00000295550.4:p.Asn2857Tyr
ENST00000295550.8:c.8569A>T	ENSP00000295550.4:p.Asn2857Tyr
ENST00000347401.7:c.6745A>T	ENSP00000315609.4:p.Asn2249Tyr
ENST00000353578.8:c.7951A>T	ENSP00000315873.4:p.Asn2651Tyr
ENST00000409809.5:c.7951A>T	ENSP00000386844.1:p.Asn2651Tyr
ENST00000472056.5:c.6748A>T	ENSP00000418285.1:p.Asn2250Tyr
ENST00000491769.1:n.5011A>T
NM_004369.3:c.8569A>T , LRG_473t1:c.8569A>T	NP_004360.2:p.Asn2857Tyr
NM_057166.4:c.6748A>T	NP_476507.3:p.Asn2250Tyr
NM_057167.3:c.7951A>T	NP_476508.2:p.Asn2651Tyr
XM_005246065.1:c.7969A>T	XP_005246122.1:p.Asn2657Tyr
XM_005246066.1:c.7348A>T	XP_005246123.1:p.Asn2450Tyr
XM_006712253.1:c.8068A>T	XP_006712316.1:p.Asn2690Tyr
XM_011510574.1:c.8566A>T	XP_011508876.1:p.Asn2856Tyr
XM_011510575.1:c.6163A>T	XP_011508877.1:p.Asn2055Tyr
XM_017003304.1:c.6163A>T	XP_016858793.1:p.Asn2055Tyr
XM_024452684.1:c.7348A>T	XP_024308452.1:p.Asn2450Tyr
NM_004369.4:c.8569A>T MANE Select	NP_004360.2:p.Asn2857Tyr
NM_057166.5:c.6748A>T	NP_476507.3:p.Asn2250Tyr
NM_057167.4:c.7951A>T	NP_476508.2:p.Asn2651Tyr