Canonical Allele Identifier: CA363616152

Gene: COL11A2

Linked Data

• dbSNP Id: rs1438657901
• gnomAD v2: 6-33132138-G-A
• MyVariant Identifiers: chr6:g.33132138G>A (hg19) ; chr6:g.33164361G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.782C>T
ENST00000341947.7:c.4976C>T MANE Select	ENSP00000339915.2:p.Ala1659Val
ENST00000341947.6:c.4976C>T	ENSP00000339915.2:p.Ala1659Val
ENST00000361917.5:c.4655C>T	ENSP00000355123.1:p.Ala1552Val
ENST00000374708.8:c.4718C>T	ENSP00000363840.4:p.Ala1573Val
ENST00000477772.1:n.766C>T
NM_080679.2:c.4655C>T	NP_542410.2:p.Ala1552Val
NM_080680.2:c.4976C>T	NP_542411.2:p.Ala1659Val
NM_080681.2:c.4718C>T	NP_542412.2:p.Ala1573Val
XM_011514298.1:c.4130C>T	XP_011512600.1:p.Ala1377Val
XM_011514299.1:c.4262C>T	XP_011512601.1:p.Ala1421Val
XM_011514300.1:c.4082C>T	XP_011512602.1:p.Ala1361Val
XM_011514301.1:c.4019C>T	XP_011512603.1:p.Ala1340Val
XM_011514302.1:c.3863C>T	XP_011512604.1:p.Ala1288Val
XM_011514299.2:c.4262C>T	XP_011512601.1:p.Ala1421Val
XM_011514300.2:c.4082C>T	XP_011512602.1:p.Ala1361Val
XM_011514302.2:c.3863C>T	XP_011512604.1:p.Ala1288Val
XM_017010250.1:c.4976C>T	XP_016865739.1:p.Ala1659Val
XM_017010251.2:c.3794C>T	XP_016865740.1:p.Ala1265Val
NM_080680.3:c.4976C>T MANE Select	NP_542411.2:p.Ala1659Val
NM_080681.3:c.4718C>T	NP_542412.2:p.Ala1573Val
NM_080679.3:c.4655C>T	NP_542410.2:p.Ala1552Val