Canonical Allele Identifier: CA2188602

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237365843A>G , CM000664.2:g.237365843A>G	GRCh38
NC_000002.11:g.238274486A>G , CM000664.1:g.238274486A>G	GRCh37
NC_000002.10:g.237939225A>G	NCBI36
NG_008676.1:g.53365T>C , LRG_473:g.53365T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004369.4:c.5693T>C MANE Select	NP_004360.2:p.Val1898Ala
ENST00000295550.9:c.5693T>C MANE Select	ENSP00000295550.4:p.Val1898Ala
NM_004369.3:c.5693T>C , LRG_473t1:c.5693T>C	NP_004360.2:p.Val1898Ala
NM_057166.4:c.3872T>C	NP_476507.3:p.Val1291Ala
NM_057166.5:c.3872T>C	NP_476507.3:p.Val1291Ala
NM_057167.3:c.5075T>C	NP_476508.2:p.Val1692Ala
NM_057167.4:c.5075T>C	NP_476508.2:p.Val1692Ala
ENST00000295550.8:c.5693T>C	ENSP00000295550.4:p.Val1898Ala
ENST00000347401.7:c.3872T>C	ENSP00000315609.4:p.Val1291Ala
ENST00000353578.8:c.5075T>C	ENSP00000315873.4:p.Val1692Ala
ENST00000353578.9:c.5075T>C	ENSP00000315873.4:p.Val1692Ala
ENST00000409809.5:c.5075T>C	ENSP00000386844.1:p.Val1692Ala
ENST00000472056.5:c.3872T>C	ENSP00000418285.1:p.Val1291Ala
XM_005246065.1:c.5093T>C	XP_005246122.1:p.Val1698Ala
XM_005246066.1:c.4472T>C	XP_005246123.1:p.Val1491Ala
XM_006712253.1:c.5192T>C	XP_006712316.1:p.Val1731Ala
XM_011510574.1:c.5690T>C	XP_011508876.1:p.Val1897Ala
XM_011510575.1:c.3287T>C	XP_011508877.1:p.Val1096Ala
XM_017003304.1:c.3287T>C	XP_016858793.1:p.Val1096Ala
XM_024452684.1:c.4472T>C	XP_024308452.1:p.Val1491Ala