Canonical Allele Identifier: CA341170147

Gene: COL11A1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102998315G>C , CM000663.2:g.102998315G>C	GRCh38
NC_000001.10:g.103463871G>C , CM000663.1:g.103463871G>C	GRCh37
NC_000001.9:g.103236459G>C	NCBI36
NG_008033.1:g.115182C>G
NG_008033.2:g.115182C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2191C>G MANE Select	ENSP00000359114.3:p.Pro731Ala
ENST00000353414.8:c.2074C>G	ENSP00000302551.6:p.Pro692Ala
ENST00000358392.6:c.2227C>G	ENSP00000351163.2:p.Pro743Ala
ENST00000370096.7:c.2191C>G	ENSP00000359114.3:p.Pro731Ala
ENST00000512756.5:c.1843C>G	ENSP00000426533.1:p.Pro615Ala
ENST00000635193.1:c.1509C>G
NM_001190709.1:c.2074C>G	NP_001177638.1:p.Pro692Ala
NM_001854.3:c.2191C>G	NP_001845.3:p.Pro731Ala
NM_080629.2:c.2227C>G	NP_542196.2:p.Pro743Ala
NM_080630.3:c.1843C>G	NP_542197.3:p.Pro615Ala
XM_011540719.1:c.2191C>G	XP_011539021.1:p.Pro731Ala
XM_011540720.1:c.424C>G	XP_011539022.1:p.Pro142Ala
XM_011540721.1:c.-238C>G	XP_011539023.1:n.-238C>G
XR_946545.1:n.2589C>G
NR_134980.1:n.2509C>G
XM_017000334.1:c.2344C>G	XP_016855823.1:p.Pro782Ala
XM_017000335.1:c.2338C>G	XP_016855824.1:p.Pro780Ala
XM_017000336.1:c.2344C>G	XP_016855825.1:p.Pro782Ala
XM_017000337.1:c.742C>G	XP_016855826.1:p.Pro248Ala
NM_001854.4:c.2191C>G MANE Select	NP_001845.3:p.Pro731Ala
NM_080630.4:c.1843C>G	NP_542197.3:p.Pro615Ala
NR_134980.2:n.2535C>G
NM_001190709.2:c.2074C>G	NP_001177638.1:p.Pro692Ala
NM_080629.3:c.2227C>G	NP_542196.2:p.Pro743Ala