Canonical Allele Identifier: CA351187739
Gene: COL6A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237366871T>A , CM000664.2:g.237366871T>A GRCh38
NC_000002.11:g.238275514T>A , CM000664.1:g.238275514T>A GRCh37
NC_000002.10:g.237940253T>A NCBI36
NG_008676.1:g.52337A>T , LRG_473:g.52337A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000353578.9:c.4698A>T ENSP00000315873.4:p.Lys1566Asn
ENST00000295550.9:c.5316A>T MANE Select ENSP00000295550.4:p.Lys1772Asn
ENST00000295550.8:c.5316A>T ENSP00000295550.4:p.Lys1772Asn
ENST00000347401.7:c.3495A>T ENSP00000315609.4:p.Lys1165Asn
ENST00000353578.8:c.4698A>T ENSP00000315873.4:p.Lys1566Asn
ENST00000409809.5:c.4698A>T ENSP00000386844.1:p.Lys1566Asn
ENST00000472056.5:c.3495A>T ENSP00000418285.1:p.Lys1165Asn
NM_004369.3:c.5316A>T , LRG_473t1:c.5316A>T NP_004360.2:p.Lys1772Asn
NM_057166.4:c.3495A>T NP_476507.3:p.Lys1165Asn
NM_057167.3:c.4698A>T NP_476508.2:p.Lys1566Asn
XM_005246065.1:c.4716A>T XP_005246122.1:p.Lys1572Asn
XM_005246066.1:c.4095A>T XP_005246123.1:p.Lys1365Asn
XM_006712253.1:c.4815A>T XP_006712316.1:p.Lys1605Asn
XM_011510574.1:c.5313A>T XP_011508876.1:p.Lys1771Asn
XM_011510575.1:c.2910A>T XP_011508877.1:p.Lys970Asn
XM_017003304.1:c.2910A>T XP_016858793.1:p.Lys970Asn
XM_024452684.1:c.4095A>T XP_024308452.1:p.Lys1365Asn
NM_004369.4:c.5316A>T MANE Select NP_004360.2:p.Lys1772Asn
NM_057166.5:c.3495A>T NP_476507.3:p.Lys1165Asn
NM_057167.4:c.4698A>T NP_476508.2:p.Lys1566Asn