Canonical Allele Identifier: CA363616308

Gene: COL11A2

Linked Data

• gnomAD v4: 6-33164389-C-T
• MyVariant Identifiers: chr6:g.33132166C>T (hg19) ; chr6:g.33164389C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164389C>T , CM000668.2:g.33164389C>T	GRCh38
NC_000006.11:g.33132166C>T , CM000668.1:g.33132166C>T	GRCh37
NC_000006.10:g.33240144C>T	NCBI36
NG_011589.1:g.33080G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.754G>A
ENST00000341947.7:c.4948G>A MANE Select	ENSP00000339915.2:p.Asp1650Asn
ENST00000341947.6:c.4948G>A	ENSP00000339915.2:p.Asp1650Asn
ENST00000361917.5:c.4627G>A	ENSP00000355123.1:p.Asp1543Asn
ENST00000374708.8:c.4690G>A	ENSP00000363840.4:p.Asp1564Asn
ENST00000477772.1:n.738G>A
NM_080679.2:c.4627G>A	NP_542410.2:p.Asp1543Asn
NM_080680.2:c.4948G>A	NP_542411.2:p.Asp1650Asn
NM_080681.2:c.4690G>A	NP_542412.2:p.Asp1564Asn
XM_011514298.1:c.4102G>A	XP_011512600.1:p.Asp1368Asn
XM_011514299.1:c.4234G>A	XP_011512601.1:p.Asp1412Asn
XM_011514300.1:c.4054G>A	XP_011512602.1:p.Asp1352Asn
XM_011514301.1:c.3991G>A	XP_011512603.1:p.Asp1331Asn
XM_011514302.1:c.3835G>A	XP_011512604.1:p.Asp1279Asn
XM_011514299.2:c.4234G>A	XP_011512601.1:p.Asp1412Asn
XM_011514300.2:c.4054G>A	XP_011512602.1:p.Asp1352Asn
XM_011514302.2:c.3835G>A	XP_011512604.1:p.Asp1279Asn
XM_017010250.1:c.4948G>A	XP_016865739.1:p.Asp1650Asn
XM_017010251.2:c.3766G>A	XP_016865740.1:p.Asp1256Asn
NM_080680.3:c.4948G>A MANE Select	NP_542411.2:p.Asp1650Asn
NM_080681.3:c.4690G>A	NP_542412.2:p.Asp1564Asn
NM_080679.3:c.4627G>A	NP_542410.2:p.Asp1543Asn