Canonical Allele Identifier: CA351191414

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244930G>A (hg19) ; chr2:g.237336287G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336287G>A , CM000664.2:g.237336287G>A	GRCh38
NC_000002.11:g.238244930G>A , CM000664.1:g.238244930G>A	GRCh37
NC_000002.10:g.237909669G>A	NCBI36
NG_008676.1:g.82921C>T , LRG_473:g.82921C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1458C>T
ENST00000353578.9:c.8195C>T	ENSP00000315873.4:p.Pro2732Leu
ENST00000682957.1:c.940C>T
ENST00000684508.1:n.1080C>T
ENST00000295550.9:c.8813C>T MANE Select	ENSP00000295550.4:p.Pro2938Leu
ENST00000295550.8:c.8813C>T	ENSP00000295550.4:p.Pro2938Leu
ENST00000347401.7:c.6989C>T	ENSP00000315609.4:p.Pro2330Leu
ENST00000353578.8:c.8195C>T	ENSP00000315873.4:p.Pro2732Leu
ENST00000409809.5:c.8195C>T	ENSP00000386844.1:p.Pro2732Leu
ENST00000472056.5:c.6992C>T	ENSP00000418285.1:p.Pro2331Leu
ENST00000491769.1:n.5255C>T
NM_004369.3:c.8813C>T , LRG_473t1:c.8813C>T	NP_004360.2:p.Pro2938Leu
NM_057166.4:c.6992C>T	NP_476507.3:p.Pro2331Leu
NM_057167.3:c.8195C>T	NP_476508.2:p.Pro2732Leu
XM_005246065.1:c.8213C>T	XP_005246122.1:p.Pro2738Leu
XM_005246066.1:c.7592C>T	XP_005246123.1:p.Pro2531Leu
XM_006712253.1:c.8312C>T	XP_006712316.1:p.Pro2771Leu
XM_011510574.1:c.8810C>T	XP_011508876.1:p.Pro2937Leu
XM_011510575.1:c.6407C>T	XP_011508877.1:p.Pro2136Leu
XM_017003304.1:c.6407C>T	XP_016858793.1:p.Pro2136Leu
XM_024452684.1:c.7592C>T	XP_024308452.1:p.Pro2531Leu
NM_004369.4:c.8813C>T MANE Select	NP_004360.2:p.Pro2938Leu
NM_057166.5:c.6992C>T	NP_476507.3:p.Pro2331Leu
NM_057167.4:c.8195C>T	NP_476508.2:p.Pro2732Leu