Canonical Allele Identifier: CA363617647

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132696A>G (hg19) ; chr6:g.33164919A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164919A>G , CM000668.2:g.33164919A>G	GRCh38
NC_000006.11:g.33132696A>G , CM000668.1:g.33132696A>G	GRCh37
NC_000006.10:g.33240674A>G	NCBI36
NG_011589.1:g.32550T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.602T>C
ENST00000341947.7:c.4796T>C MANE Select	ENSP00000339915.2:p.Phe1599Ser
ENST00000341947.6:c.4796T>C	ENSP00000339915.2:p.Phe1599Ser
ENST00000361917.5:c.4475T>C	ENSP00000355123.1:p.Phe1492Ser
ENST00000374708.8:c.4538T>C	ENSP00000363840.4:p.Phe1513Ser
ENST00000477772.1:n.586T>C
NM_080679.2:c.4475T>C	NP_542410.2:p.Phe1492Ser
NM_080680.2:c.4796T>C	NP_542411.2:p.Phe1599Ser
NM_080681.2:c.4538T>C	NP_542412.2:p.Phe1513Ser
XM_011514298.1:c.3950T>C	XP_011512600.1:p.Phe1317Ser
XM_011514299.1:c.4082T>C	XP_011512601.1:p.Phe1361Ser
XM_011514300.1:c.3902T>C	XP_011512602.1:p.Phe1301Ser
XM_011514301.1:c.3839T>C	XP_011512603.1:p.Phe1280Ser
XM_011514302.1:c.3683T>C	XP_011512604.1:p.Phe1228Ser
XM_011514299.2:c.4082T>C	XP_011512601.1:p.Phe1361Ser
XM_011514300.2:c.3902T>C	XP_011512602.1:p.Phe1301Ser
XM_011514302.2:c.3683T>C	XP_011512604.1:p.Phe1228Ser
XM_017010250.1:c.4796T>C	XP_016865739.1:p.Phe1599Ser
XM_017010251.2:c.3614T>C	XP_016865740.1:p.Phe1205Ser
NM_080680.3:c.4796T>C MANE Select	NP_542411.2:p.Phe1599Ser
NM_080681.3:c.4538T>C	NP_542412.2:p.Phe1513Ser
NM_080679.3:c.4475T>C	NP_542410.2:p.Phe1492Ser