Canonical Allele Identifier: CA341163443

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444466G>C (hg19) ; chr1:g.102978910G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978910G>C , CM000663.2:g.102978910G>C	GRCh38
NC_000001.10:g.103444466G>C , CM000663.1:g.103444466G>C	GRCh37
NC_000001.9:g.103217054G>C	NCBI36
NG_008033.1:g.134587C>G
NG_008033.2:g.134587C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2659C>G MANE Select	ENSP00000359114.3:p.Pro887Ala
ENST00000353414.8:c.2542C>G	ENSP00000302551.6:p.Pro848Ala
ENST00000358392.6:c.2695C>G	ENSP00000351163.2:p.Pro899Ala
ENST00000370096.7:c.2659C>G	ENSP00000359114.3:p.Pro887Ala
ENST00000512756.5:c.2311C>G	ENSP00000426533.1:p.Pro771Ala
ENST00000635193.1:c.1993C>G
NM_001190709.1:c.2542C>G	NP_001177638.1:p.Pro848Ala
NM_001854.3:c.2659C>G	NP_001845.3:p.Pro887Ala
NM_080629.2:c.2695C>G	NP_542196.2:p.Pro899Ala
NM_080630.3:c.2311C>G	NP_542197.3:p.Pro771Ala
XM_011540719.1:c.2659C>G	XP_011539021.1:p.Pro887Ala
XM_011540720.1:c.892C>G	XP_011539022.1:p.Pro298Ala
XM_011540721.1:c.247C>G	XP_011539023.1:p.Pro83Ala
XR_946545.1:n.3073C>G
NR_134980.1:n.2993C>G
XM_017000334.1:c.2812C>G	XP_016855823.1:p.Pro938Ala
XM_017000335.1:c.2806C>G	XP_016855824.1:p.Pro936Ala
XM_017000336.1:c.2812C>G	XP_016855825.1:p.Pro938Ala
XM_017000337.1:c.1210C>G	XP_016855826.1:p.Pro404Ala
NM_001854.4:c.2659C>G MANE Select	NP_001845.3:p.Pro887Ala
NM_080630.4:c.2311C>G	NP_542197.3:p.Pro771Ala
NR_134980.2:n.3019C>G
NM_001190709.2:c.2542C>G	NP_001177638.1:p.Pro848Ala
NM_080629.3:c.2695C>G	NP_542196.2:p.Pro899Ala