Canonical Allele Identifier: CA419200227

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444437G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978881G>C , CM000663.2:g.102978881G>C	GRCh38
NC_000001.10:g.103444437G>C , CM000663.1:g.103444437G>C	GRCh37
NC_000001.9:g.103217025G>C	NCBI36
NG_008033.1:g.134616C>G
NG_008033.2:g.134616C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2688C>G MANE Select	ENSP00000359114.3:p.Pro896=
ENST00000353414.8:c.2571C>G	ENSP00000302551.6:p.Pro857=
ENST00000358392.6:c.2724C>G	ENSP00000351163.2:p.Pro908=
ENST00000370096.7:c.2688C>G	ENSP00000359114.3:p.Pro896=
ENST00000512756.5:c.2340C>G	ENSP00000426533.1:p.Pro780=
ENST00000635193.1:c.2022C>G
NM_001190709.1:c.2571C>G	NP_001177638.1:p.Pro857=
NM_001854.3:c.2688C>G	NP_001845.3:p.Pro896=
NM_080629.2:c.2724C>G	NP_542196.2:p.Pro908=
NM_080630.3:c.2340C>G	NP_542197.3:p.Pro780=
XM_011540719.1:c.2688C>G	XP_011539021.1:p.Pro896=
XM_011540720.1:c.921C>G	XP_011539022.1:p.Pro307=
XM_011540721.1:c.276C>G	XP_011539023.1:p.Pro92=
XR_946545.1:n.3102C>G
NR_134980.1:n.3022C>G
XM_017000334.1:c.2841C>G	XP_016855823.1:p.Pro947=
XM_017000335.1:c.2835C>G	XP_016855824.1:p.Pro945=
XM_017000336.1:c.2841C>G	XP_016855825.1:p.Pro947=
XM_017000337.1:c.1239C>G	XP_016855826.1:p.Pro413=
NM_001854.4:c.2688C>G MANE Select	NP_001845.3:p.Pro896=
NM_080630.4:c.2340C>G	NP_542197.3:p.Pro780=
NR_134980.2:n.3048C>G
NM_001190709.2:c.2571C>G	NP_001177638.1:p.Pro857=
NM_080629.3:c.2724C>G	NP_542196.2:p.Pro908=