Canonical Allele Identifier: CA449872155

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33137238T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33169461T>G , CM000668.2:g.33169461T>G	GRCh38
NC_000006.11:g.33137238T>G , CM000668.1:g.33137238T>G	GRCh37
NC_000006.10:g.33245216T>G	NCBI36
NG_011589.1:g.28008A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341947.7:c.3720A>C MANE Select	ENSP00000339915.2:p.Gly1240=
ENST00000341947.6:c.3720A>C	ENSP00000339915.2:p.Gly1240=
ENST00000361917.5:c.3399A>C	ENSP00000355123.1:p.Gly1133=
ENST00000374708.8:c.3462A>C	ENSP00000363840.4:p.Gly1154=
ENST00000477772.1:n.273-3645A>C
NM_080679.2:c.3399A>C	NP_542410.2:p.Gly1133=
NM_080680.2:c.3720A>C	NP_542411.2:p.Gly1240=
NM_080681.2:c.3462A>C	NP_542412.2:p.Gly1154=
XM_011514298.1:c.2874A>C	XP_011512600.1:p.Gly958=
XM_011514299.1:c.3006A>C	XP_011512601.1:p.Gly1002=
XM_011514300.1:c.2826A>C	XP_011512602.1:p.Gly942=
XM_011514301.1:c.2763A>C	XP_011512603.1:p.Gly921=
XM_011514302.1:c.2607A>C	XP_011512604.1:p.Gly869=
XM_011514299.2:c.3006A>C	XP_011512601.1:p.Gly1002=
XM_011514300.2:c.2826A>C	XP_011512602.1:p.Gly942=
XM_011514302.2:c.2607A>C	XP_011512604.1:p.Gly869=
XM_017010250.1:c.3720A>C	XP_016865739.1:p.Gly1240=
XM_017010251.2:c.2538A>C	XP_016865740.1:p.Gly846=
NM_080680.3:c.3720A>C MANE Select	NP_542411.2:p.Gly1240=
NM_080681.3:c.3462A>C	NP_542412.2:p.Gly1154=
NM_080679.3:c.3399A>C	NP_542410.2:p.Gly1133=