Canonical Allele Identifier: CA363616493

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132207T>A (hg19) ; chr6:g.33164430T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164430T>A , CM000668.2:g.33164430T>A	GRCh38
NC_000006.11:g.33132207T>A , CM000668.1:g.33132207T>A	GRCh37
NC_000006.10:g.33240185T>A	NCBI36
NG_011589.1:g.33039A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.713A>T
ENST00000341947.7:c.4907A>T MANE Select	ENSP00000339915.2:p.Gln1636Leu
ENST00000341947.6:c.4907A>T	ENSP00000339915.2:p.Gln1636Leu
ENST00000361917.5:c.4586A>T	ENSP00000355123.1:p.Gln1529Leu
ENST00000374708.8:c.4649A>T	ENSP00000363840.4:p.Gln1550Leu
ENST00000477772.1:n.697A>T
NM_080679.2:c.4586A>T	NP_542410.2:p.Gln1529Leu
NM_080680.2:c.4907A>T	NP_542411.2:p.Gln1636Leu
NM_080681.2:c.4649A>T	NP_542412.2:p.Gln1550Leu
XM_011514298.1:c.4061A>T	XP_011512600.1:p.Gln1354Leu
XM_011514299.1:c.4193A>T	XP_011512601.1:p.Gln1398Leu
XM_011514300.1:c.4013A>T	XP_011512602.1:p.Gln1338Leu
XM_011514301.1:c.3950A>T	XP_011512603.1:p.Gln1317Leu
XM_011514302.1:c.3794A>T	XP_011512604.1:p.Gln1265Leu
XM_011514299.2:c.4193A>T	XP_011512601.1:p.Gln1398Leu
XM_011514300.2:c.4013A>T	XP_011512602.1:p.Gln1338Leu
XM_011514302.2:c.3794A>T	XP_011512604.1:p.Gln1265Leu
XM_017010250.1:c.4907A>T	XP_016865739.1:p.Gln1636Leu
XM_017010251.2:c.3725A>T	XP_016865740.1:p.Gln1242Leu
NM_080680.3:c.4907A>T MANE Select	NP_542411.2:p.Gln1636Leu
NM_080681.3:c.4649A>T	NP_542412.2:p.Gln1550Leu
NM_080679.3:c.4586A>T	NP_542410.2:p.Gln1529Leu