Canonical Allele Identifier: CA363616256

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132159G>T (hg19) ; chr6:g.33164382G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164382G>T , CM000668.2:g.33164382G>T	GRCh38
NC_000006.11:g.33132159G>T , CM000668.1:g.33132159G>T	GRCh37
NC_000006.10:g.33240137G>T	NCBI36
NG_011589.1:g.33087C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.761C>A
ENST00000341947.7:c.4955C>A MANE Select	ENSP00000339915.2:p.Ser1652Tyr
ENST00000341947.6:c.4955C>A	ENSP00000339915.2:p.Ser1652Tyr
ENST00000361917.5:c.4634C>A	ENSP00000355123.1:p.Ser1545Tyr
ENST00000374708.8:c.4697C>A	ENSP00000363840.4:p.Ser1566Tyr
ENST00000477772.1:n.745C>A
NM_080679.2:c.4634C>A	NP_542410.2:p.Ser1545Tyr
NM_080680.2:c.4955C>A	NP_542411.2:p.Ser1652Tyr
NM_080681.2:c.4697C>A	NP_542412.2:p.Ser1566Tyr
XM_011514298.1:c.4109C>A	XP_011512600.1:p.Ser1370Tyr
XM_011514299.1:c.4241C>A	XP_011512601.1:p.Ser1414Tyr
XM_011514300.1:c.4061C>A	XP_011512602.1:p.Ser1354Tyr
XM_011514301.1:c.3998C>A	XP_011512603.1:p.Ser1333Tyr
XM_011514302.1:c.3842C>A	XP_011512604.1:p.Ser1281Tyr
XM_011514299.2:c.4241C>A	XP_011512601.1:p.Ser1414Tyr
XM_011514300.2:c.4061C>A	XP_011512602.1:p.Ser1354Tyr
XM_011514302.2:c.3842C>A	XP_011512604.1:p.Ser1281Tyr
XM_017010250.1:c.4955C>A	XP_016865739.1:p.Ser1652Tyr
XM_017010251.2:c.3773C>A	XP_016865740.1:p.Ser1258Tyr
NM_080680.3:c.4955C>A MANE Select	NP_542411.2:p.Ser1652Tyr
NM_080681.3:c.4697C>A	NP_542412.2:p.Ser1566Tyr
NM_080679.3:c.4634C>A	NP_542410.2:p.Ser1545Tyr