Canonical Allele Identifier: CA913047087

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444604C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979048C>G , CM000663.2:g.102979048C>G	GRCh38
NC_000001.10:g.103444604C>G , CM000663.1:g.103444604C>G	GRCh37
NC_000001.9:g.103217192C>G	NCBI36
NG_008033.1:g.134449G>C
NG_008033.2:g.134449G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2655+12G>C MANE Select	ENSP00000359114.3:n.2655+12G>C
ENST00000353414.8:c.2538+12G>C	ENSP00000302551.6:n.2538+12G>C
ENST00000358392.6:c.2691+12G>C	ENSP00000351163.2:n.2691+12G>C
ENST00000370096.7:c.2655+12G>C	ENSP00000359114.3:n.2655+12G>C
ENST00000512756.5:c.2307+12G>C	ENSP00000426533.1:n.2307+12G>C
ENST00000635193.1:c.1989+12G>C
NM_001190709.1:c.2538+12G>C	NP_001177638.1:n.2538+12G>C
NM_001854.3:c.2655+12G>C	NP_001845.3:n.2655+12G>C
NM_080629.2:c.2691+12G>C	NP_542196.2:n.2691+12G>C
NM_080630.3:c.2307+12G>C	NP_542197.3:n.2307+12G>C
XM_011540719.1:c.2655+12G>C	XP_011539021.1:n.2655+12G>C
XM_011540720.1:c.888+12G>C	XP_011539022.1:n.888+12G>C
XM_011540721.1:c.243+12G>C	XP_011539023.1:n.243+12G>C
XR_946545.1:n.3069+12G>C
NR_134980.1:n.2989+12G>C
XM_017000334.1:c.2808+12G>C	XP_016855823.1:n.2808+12G>C
XM_017000335.1:c.2802+12G>C	XP_016855824.1:n.2802+12G>C
XM_017000336.1:c.2808+12G>C	XP_016855825.1:n.2808+12G>C
XM_017000337.1:c.1206+12G>C	XP_016855826.1:n.1206+12G>C
NM_001854.4:c.2655+12G>C MANE Select	NP_001845.3:n.2655+12G>C
NM_080630.4:c.2307+12G>C	NP_542197.3:n.2307+12G>C
NR_134980.2:n.3015+12G>C
NM_001190709.2:c.2538+12G>C	NP_001177638.1:n.2538+12G>C
NM_080629.3:c.2691+12G>C	NP_542196.2:n.2691+12G>C