Canonical Allele Identifier: CA363616302

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132165T>G (hg19) ; chr6:g.33164388T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164388T>G , CM000668.2:g.33164388T>G	GRCh38
NC_000006.11:g.33132165T>G , CM000668.1:g.33132165T>G	GRCh37
NC_000006.10:g.33240143T>G	NCBI36
NG_011589.1:g.33081A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.755A>C
ENST00000341947.7:c.4949A>C MANE Select	ENSP00000339915.2:p.Asp1650Ala
ENST00000341947.6:c.4949A>C	ENSP00000339915.2:p.Asp1650Ala
ENST00000361917.5:c.4628A>C	ENSP00000355123.1:p.Asp1543Ala
ENST00000374708.8:c.4691A>C	ENSP00000363840.4:p.Asp1564Ala
ENST00000477772.1:n.739A>C
NM_080679.2:c.4628A>C	NP_542410.2:p.Asp1543Ala
NM_080680.2:c.4949A>C	NP_542411.2:p.Asp1650Ala
NM_080681.2:c.4691A>C	NP_542412.2:p.Asp1564Ala
XM_011514298.1:c.4103A>C	XP_011512600.1:p.Asp1368Ala
XM_011514299.1:c.4235A>C	XP_011512601.1:p.Asp1412Ala
XM_011514300.1:c.4055A>C	XP_011512602.1:p.Asp1352Ala
XM_011514301.1:c.3992A>C	XP_011512603.1:p.Asp1331Ala
XM_011514302.1:c.3836A>C	XP_011512604.1:p.Asp1279Ala
XM_011514299.2:c.4235A>C	XP_011512601.1:p.Asp1412Ala
XM_011514300.2:c.4055A>C	XP_011512602.1:p.Asp1352Ala
XM_011514302.2:c.3836A>C	XP_011512604.1:p.Asp1279Ala
XM_017010250.1:c.4949A>C	XP_016865739.1:p.Asp1650Ala
XM_017010251.2:c.3767A>C	XP_016865740.1:p.Asp1256Ala
NM_080680.3:c.4949A>C MANE Select	NP_542411.2:p.Asp1650Ala
NM_080681.3:c.4691A>C	NP_542412.2:p.Asp1564Ala
NM_080679.3:c.4628A>C	NP_542410.2:p.Asp1543Ala