Canonical Allele Identifier: CA449867014

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132173G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164396G>C , CM000668.2:g.33164396G>C	GRCh38
NC_000006.11:g.33132173G>C , CM000668.1:g.33132173G>C	GRCh37
NC_000006.10:g.33240151G>C	NCBI36
NG_011589.1:g.33073C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.747C>G
ENST00000341947.7:c.4941C>G MANE Select	ENSP00000339915.2:p.Ala1647=
ENST00000341947.6:c.4941C>G	ENSP00000339915.2:p.Ala1647=
ENST00000361917.5:c.4620C>G	ENSP00000355123.1:p.Ala1540=
ENST00000374708.8:c.4683C>G	ENSP00000363840.4:p.Ala1561=
ENST00000477772.1:n.731C>G
NM_080679.2:c.4620C>G	NP_542410.2:p.Ala1540=
NM_080680.2:c.4941C>G	NP_542411.2:p.Ala1647=
NM_080681.2:c.4683C>G	NP_542412.2:p.Ala1561=
XM_011514298.1:c.4095C>G	XP_011512600.1:p.Ala1365=
XM_011514299.1:c.4227C>G	XP_011512601.1:p.Ala1409=
XM_011514300.1:c.4047C>G	XP_011512602.1:p.Ala1349=
XM_011514301.1:c.3984C>G	XP_011512603.1:p.Ala1328=
XM_011514302.1:c.3828C>G	XP_011512604.1:p.Ala1276=
XM_011514299.2:c.4227C>G	XP_011512601.1:p.Ala1409=
XM_011514300.2:c.4047C>G	XP_011512602.1:p.Ala1349=
XM_011514302.2:c.3828C>G	XP_011512604.1:p.Ala1276=
XM_017010250.1:c.4941C>G	XP_016865739.1:p.Ala1647=
XM_017010251.2:c.3759C>G	XP_016865740.1:p.Ala1253=
NM_080680.3:c.4941C>G MANE Select	NP_542411.2:p.Ala1647=
NM_080681.3:c.4683C>G	NP_542412.2:p.Ala1561=
NM_080679.3:c.4620C>G	NP_542410.2:p.Ala1540=