Canonical Allele Identifier: CA449867088

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132248G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164471G>A , CM000668.2:g.33164471G>A	GRCh38
NC_000006.11:g.33132248G>A , CM000668.1:g.33132248G>A	GRCh37
NC_000006.10:g.33240226G>A	NCBI36
NG_011589.1:g.32998C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.672C>T
ENST00000341947.7:c.4866C>T MANE Select	ENSP00000339915.2:p.Phe1622=
ENST00000341947.6:c.4866C>T	ENSP00000339915.2:p.Phe1622=
ENST00000361917.5:c.4545C>T	ENSP00000355123.1:p.Phe1515=
ENST00000374708.8:c.4608C>T	ENSP00000363840.4:p.Phe1536=
ENST00000477772.1:n.656C>T
NM_080679.2:c.4545C>T	NP_542410.2:p.Phe1515=
NM_080680.2:c.4866C>T	NP_542411.2:p.Phe1622=
NM_080681.2:c.4608C>T	NP_542412.2:p.Phe1536=
XM_011514298.1:c.4020C>T	XP_011512600.1:p.Phe1340=
XM_011514299.1:c.4152C>T	XP_011512601.1:p.Phe1384=
XM_011514300.1:c.3972C>T	XP_011512602.1:p.Phe1324=
XM_011514301.1:c.3909C>T	XP_011512603.1:p.Phe1303=
XM_011514302.1:c.3753C>T	XP_011512604.1:p.Phe1251=
XM_011514299.2:c.4152C>T	XP_011512601.1:p.Phe1384=
XM_011514300.2:c.3972C>T	XP_011512602.1:p.Phe1324=
XM_011514302.2:c.3753C>T	XP_011512604.1:p.Phe1251=
XM_017010250.1:c.4866C>T	XP_016865739.1:p.Phe1622=
XM_017010251.2:c.3684C>T	XP_016865740.1:p.Phe1228=
NM_080680.3:c.4866C>T MANE Select	NP_542411.2:p.Phe1622=
NM_080681.3:c.4608C>T	NP_542412.2:p.Phe1536=
NM_080679.3:c.4545C>T	NP_542410.2:p.Phe1515=