Canonical Allele Identifier: CA341163760

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444656A>C (hg19) ; chr1:g.102979100A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979100A>C , CM000663.2:g.102979100A>C	GRCh38
NC_000001.10:g.103444656A>C , CM000663.1:g.103444656A>C	GRCh37
NC_000001.9:g.103217244A>C	NCBI36
NG_008033.1:g.134397T>G
NG_008033.2:g.134397T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2615T>G MANE Select	ENSP00000359114.3:p.Val872Gly
ENST00000353414.8:c.2498T>G	ENSP00000302551.6:p.Val833Gly
ENST00000358392.6:c.2651T>G	ENSP00000351163.2:p.Val884Gly
ENST00000370096.7:c.2615T>G	ENSP00000359114.3:p.Val872Gly
ENST00000512756.5:c.2267T>G	ENSP00000426533.1:p.Val756Gly
ENST00000635193.1:c.1949T>G
NM_001190709.1:c.2498T>G	NP_001177638.1:p.Val833Gly
NM_001854.3:c.2615T>G	NP_001845.3:p.Val872Gly
NM_080629.2:c.2651T>G	NP_542196.2:p.Val884Gly
NM_080630.3:c.2267T>G	NP_542197.3:p.Val756Gly
XM_011540719.1:c.2615T>G	XP_011539021.1:p.Val872Gly
XM_011540720.1:c.848T>G	XP_011539022.1:p.Val283Gly
XM_011540721.1:c.203T>G	XP_011539023.1:p.Val68Gly
XR_946545.1:n.3029T>G
NR_134980.1:n.2949T>G
XM_017000334.1:c.2768T>G	XP_016855823.1:p.Val923Gly
XM_017000335.1:c.2762T>G	XP_016855824.1:p.Val921Gly
XM_017000336.1:c.2768T>G	XP_016855825.1:p.Val923Gly
XM_017000337.1:c.1166T>G	XP_016855826.1:p.Val389Gly
NM_001854.4:c.2615T>G MANE Select	NP_001845.3:p.Val872Gly
NM_080630.4:c.2267T>G	NP_542197.3:p.Val756Gly
NR_134980.2:n.2975T>G
NM_001190709.2:c.2498T>G	NP_001177638.1:p.Val833Gly
NM_080629.3:c.2651T>G	NP_542196.2:p.Val884Gly