Canonical Allele Identifier: CA341163603

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444630G>A (hg19) ; chr1:g.102979074G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979074G>A , CM000663.2:g.102979074G>A	GRCh38
NC_000001.10:g.103444630G>A , CM000663.1:g.103444630G>A	GRCh37
NC_000001.9:g.103217218G>A	NCBI36
NG_008033.1:g.134423C>T
NG_008033.2:g.134423C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2641C>T MANE Select	ENSP00000359114.3:p.Gln881Ter
ENST00000353414.8:c.2524C>T	ENSP00000302551.6:p.Gln842Ter
ENST00000358392.6:c.2677C>T	ENSP00000351163.2:p.Gln893Ter
ENST00000370096.7:c.2641C>T	ENSP00000359114.3:p.Gln881Ter
ENST00000512756.5:c.2293C>T	ENSP00000426533.1:p.Gln765Ter
ENST00000635193.1:c.1975C>T
NM_001190709.1:c.2524C>T	NP_001177638.1:p.Gln842Ter
NM_001854.3:c.2641C>T	NP_001845.3:p.Gln881Ter
NM_080629.2:c.2677C>T	NP_542196.2:p.Gln893Ter
NM_080630.3:c.2293C>T	NP_542197.3:p.Gln765Ter
XM_011540719.1:c.2641C>T	XP_011539021.1:p.Gln881Ter
XM_011540720.1:c.874C>T	XP_011539022.1:p.Gln292Ter
XM_011540721.1:c.229C>T	XP_011539023.1:p.Gln77Ter
XR_946545.1:n.3055C>T
NR_134980.1:n.2975C>T
XM_017000334.1:c.2794C>T	XP_016855823.1:p.Gln932Ter
XM_017000335.1:c.2788C>T	XP_016855824.1:p.Gln930Ter
XM_017000336.1:c.2794C>T	XP_016855825.1:p.Gln932Ter
XM_017000337.1:c.1192C>T	XP_016855826.1:p.Gln398Ter
NM_001854.4:c.2641C>T MANE Select	NP_001845.3:p.Gln881Ter
NM_080630.4:c.2293C>T	NP_542197.3:p.Gln765Ter
NR_134980.2:n.3001C>T
NM_001190709.2:c.2524C>T	NP_001177638.1:p.Gln842Ter
NM_080629.3:c.2677C>T	NP_542196.2:p.Gln893Ter