Canonical Allele Identifier: CA351216692

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238268787G>A (hg19) ; chr2:g.237360144G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237360144G>A , CM000664.2:g.237360144G>A	GRCh38
NC_000002.11:g.238268787G>A , CM000664.1:g.238268787G>A	GRCh37
NC_000002.10:g.237933526G>A	NCBI36
NG_008676.1:g.59064C>T , LRG_473:g.59064C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353578.9:c.5608C>T	ENSP00000315873.4:p.Pro1870Ser
ENST00000295550.9:c.6226C>T MANE Select	ENSP00000295550.4:p.Pro2076Ser
ENST00000295550.8:c.6226C>T	ENSP00000295550.4:p.Pro2076Ser
ENST00000347401.7:c.4405C>T	ENSP00000315609.4:p.Pro1469Ser
ENST00000353578.8:c.5608C>T	ENSP00000315873.4:p.Pro1870Ser
ENST00000409809.5:c.5608C>T	ENSP00000386844.1:p.Pro1870Ser
ENST00000472056.5:c.4405C>T	ENSP00000418285.1:p.Pro1469Ser
NM_004369.3:c.6226C>T , LRG_473t1:c.6226C>T	NP_004360.2:p.Pro2076Ser
NM_057166.4:c.4405C>T	NP_476507.3:p.Pro1469Ser
NM_057167.3:c.5608C>T	NP_476508.2:p.Pro1870Ser
XM_005246065.1:c.5626C>T	XP_005246122.1:p.Pro1876Ser
XM_005246066.1:c.5005C>T	XP_005246123.1:p.Pro1669Ser
XM_006712253.1:c.5725C>T	XP_006712316.1:p.Pro1909Ser
XM_011510574.1:c.6223C>T	XP_011508876.1:p.Pro2075Ser
XM_011510575.1:c.3820C>T	XP_011508877.1:p.Pro1274Ser
XM_017003304.1:c.3820C>T	XP_016858793.1:p.Pro1274Ser
XM_024452684.1:c.5005C>T	XP_024308452.1:p.Pro1669Ser
NM_004369.4:c.6226C>T MANE Select	NP_004360.2:p.Pro2076Ser
NM_057166.5:c.4405C>T	NP_476507.3:p.Pro1469Ser
NM_057167.4:c.5608C>T	NP_476508.2:p.Pro1870Ser