Canonical Allele Identifier: CA363616188

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132145C>T (hg19) ; chr6:g.33164368C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164368C>T , CM000668.2:g.33164368C>T	GRCh38
NC_000006.11:g.33132145C>T , CM000668.1:g.33132145C>T	GRCh37
NC_000006.10:g.33240123C>T	NCBI36
NG_011589.1:g.33101G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.775G>A
ENST00000341947.7:c.4969G>A MANE Select	ENSP00000339915.2:p.Gly1657Arg
ENST00000341947.6:c.4969G>A	ENSP00000339915.2:p.Gly1657Arg
ENST00000361917.5:c.4648G>A	ENSP00000355123.1:p.Gly1550Arg
ENST00000374708.8:c.4711G>A	ENSP00000363840.4:p.Gly1571Arg
ENST00000477772.1:n.759G>A
NM_080679.2:c.4648G>A	NP_542410.2:p.Gly1550Arg
NM_080680.2:c.4969G>A	NP_542411.2:p.Gly1657Arg
NM_080681.2:c.4711G>A	NP_542412.2:p.Gly1571Arg
XM_011514298.1:c.4123G>A	XP_011512600.1:p.Gly1375Arg
XM_011514299.1:c.4255G>A	XP_011512601.1:p.Gly1419Arg
XM_011514300.1:c.4075G>A	XP_011512602.1:p.Gly1359Arg
XM_011514301.1:c.4012G>A	XP_011512603.1:p.Gly1338Arg
XM_011514302.1:c.3856G>A	XP_011512604.1:p.Gly1286Arg
XM_011514299.2:c.4255G>A	XP_011512601.1:p.Gly1419Arg
XM_011514300.2:c.4075G>A	XP_011512602.1:p.Gly1359Arg
XM_011514302.2:c.3856G>A	XP_011512604.1:p.Gly1286Arg
XM_017010250.1:c.4969G>A	XP_016865739.1:p.Gly1657Arg
XM_017010251.2:c.3787G>A	XP_016865740.1:p.Gly1263Arg
NM_080680.3:c.4969G>A MANE Select	NP_542411.2:p.Gly1657Arg
NM_080681.3:c.4711G>A	NP_542412.2:p.Gly1571Arg
NM_080679.3:c.4648G>A	NP_542410.2:p.Gly1550Arg