Canonical Allele Identifier: CA363616515

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132213A>C (hg19) ; chr6:g.33164436A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164436A>C , CM000668.2:g.33164436A>C	GRCh38
NC_000006.11:g.33132213A>C , CM000668.1:g.33132213A>C	GRCh37
NC_000006.10:g.33240191A>C	NCBI36
NG_011589.1:g.33033T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.707T>G
ENST00000341947.7:c.4901T>G MANE Select	ENSP00000339915.2:p.Val1634Gly
ENST00000341947.6:c.4901T>G	ENSP00000339915.2:p.Val1634Gly
ENST00000361917.5:c.4580T>G	ENSP00000355123.1:p.Val1527Gly
ENST00000374708.8:c.4643T>G	ENSP00000363840.4:p.Val1548Gly
ENST00000477772.1:n.691T>G
NM_080679.2:c.4580T>G	NP_542410.2:p.Val1527Gly
NM_080680.2:c.4901T>G	NP_542411.2:p.Val1634Gly
NM_080681.2:c.4643T>G	NP_542412.2:p.Val1548Gly
XM_011514298.1:c.4055T>G	XP_011512600.1:p.Val1352Gly
XM_011514299.1:c.4187T>G	XP_011512601.1:p.Val1396Gly
XM_011514300.1:c.4007T>G	XP_011512602.1:p.Val1336Gly
XM_011514301.1:c.3944T>G	XP_011512603.1:p.Val1315Gly
XM_011514302.1:c.3788T>G	XP_011512604.1:p.Val1263Gly
XM_011514299.2:c.4187T>G	XP_011512601.1:p.Val1396Gly
XM_011514300.2:c.4007T>G	XP_011512602.1:p.Val1336Gly
XM_011514302.2:c.3788T>G	XP_011512604.1:p.Val1263Gly
XM_017010250.1:c.4901T>G	XP_016865739.1:p.Val1634Gly
XM_017010251.2:c.3719T>G	XP_016865740.1:p.Val1240Gly
NM_080680.3:c.4901T>G MANE Select	NP_542411.2:p.Val1634Gly
NM_080681.3:c.4643T>G	NP_542412.2:p.Val1548Gly
NM_080679.3:c.4580T>G	NP_542410.2:p.Val1527Gly