Canonical Allele Identifier: CA363616368

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132183C>A (hg19) ; chr6:g.33164406C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164406C>A , CM000668.2:g.33164406C>A	GRCh38
NC_000006.11:g.33132183C>A , CM000668.1:g.33132183C>A	GRCh37
NC_000006.10:g.33240161C>A	NCBI36
NG_011589.1:g.33063G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.737G>T
ENST00000341947.7:c.4931G>T MANE Select	ENSP00000339915.2:p.Ser1644Ile
ENST00000341947.6:c.4931G>T	ENSP00000339915.2:p.Ser1644Ile
ENST00000361917.5:c.4610G>T	ENSP00000355123.1:p.Ser1537Ile
ENST00000374708.8:c.4673G>T	ENSP00000363840.4:p.Ser1558Ile
ENST00000477772.1:n.721G>T
NM_080679.2:c.4610G>T	NP_542410.2:p.Ser1537Ile
NM_080680.2:c.4931G>T	NP_542411.2:p.Ser1644Ile
NM_080681.2:c.4673G>T	NP_542412.2:p.Ser1558Ile
XM_011514298.1:c.4085G>T	XP_011512600.1:p.Ser1362Ile
XM_011514299.1:c.4217G>T	XP_011512601.1:p.Ser1406Ile
XM_011514300.1:c.4037G>T	XP_011512602.1:p.Ser1346Ile
XM_011514301.1:c.3974G>T	XP_011512603.1:p.Ser1325Ile
XM_011514302.1:c.3818G>T	XP_011512604.1:p.Ser1273Ile
XM_011514299.2:c.4217G>T	XP_011512601.1:p.Ser1406Ile
XM_011514300.2:c.4037G>T	XP_011512602.1:p.Ser1346Ile
XM_011514302.2:c.3818G>T	XP_011512604.1:p.Ser1273Ile
XM_017010250.1:c.4931G>T	XP_016865739.1:p.Ser1644Ile
XM_017010251.2:c.3749G>T	XP_016865740.1:p.Ser1250Ile
NM_080680.3:c.4931G>T MANE Select	NP_542411.2:p.Ser1644Ile
NM_080681.3:c.4673G>T	NP_542412.2:p.Ser1558Ile
NM_080679.3:c.4610G>T	NP_542410.2:p.Ser1537Ile