Canonical Allele Identifier: CA363616155

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132138G>T (hg19) ; chr6:g.33164361G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164361G>T , CM000668.2:g.33164361G>T	GRCh38
NC_000006.11:g.33132138G>T , CM000668.1:g.33132138G>T	GRCh37
NC_000006.10:g.33240116G>T	NCBI36
NG_011589.1:g.33108C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.782C>A
ENST00000341947.7:c.4976C>A MANE Select	ENSP00000339915.2:p.Ala1659Asp
ENST00000341947.6:c.4976C>A	ENSP00000339915.2:p.Ala1659Asp
ENST00000361917.5:c.4655C>A	ENSP00000355123.1:p.Ala1552Asp
ENST00000374708.8:c.4718C>A	ENSP00000363840.4:p.Ala1573Asp
ENST00000477772.1:n.766C>A
NM_080679.2:c.4655C>A	NP_542410.2:p.Ala1552Asp
NM_080680.2:c.4976C>A	NP_542411.2:p.Ala1659Asp
NM_080681.2:c.4718C>A	NP_542412.2:p.Ala1573Asp
XM_011514298.1:c.4130C>A	XP_011512600.1:p.Ala1377Asp
XM_011514299.1:c.4262C>A	XP_011512601.1:p.Ala1421Asp
XM_011514300.1:c.4082C>A	XP_011512602.1:p.Ala1361Asp
XM_011514301.1:c.4019C>A	XP_011512603.1:p.Ala1340Asp
XM_011514302.1:c.3863C>A	XP_011512604.1:p.Ala1288Asp
XM_011514299.2:c.4262C>A	XP_011512601.1:p.Ala1421Asp
XM_011514300.2:c.4082C>A	XP_011512602.1:p.Ala1361Asp
XM_011514302.2:c.3863C>A	XP_011512604.1:p.Ala1288Asp
XM_017010250.1:c.4976C>A	XP_016865739.1:p.Ala1659Asp
XM_017010251.2:c.3794C>A	XP_016865740.1:p.Ala1265Asp
NM_080680.3:c.4976C>A MANE Select	NP_542411.2:p.Ala1659Asp
NM_080681.3:c.4718C>A	NP_542412.2:p.Ala1573Asp
NM_080679.3:c.4655C>A	NP_542410.2:p.Ala1552Asp