Canonical Allele Identifier: CA363616439

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132198A>G (hg19) ; chr6:g.33164421A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164421A>G , CM000668.2:g.33164421A>G	GRCh38
NC_000006.11:g.33132198A>G , CM000668.1:g.33132198A>G	GRCh37
NC_000006.10:g.33240176A>G	NCBI36
NG_011589.1:g.33048T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.722T>C
ENST00000341947.7:c.4916T>C MANE Select	ENSP00000339915.2:p.Phe1639Ser
ENST00000341947.6:c.4916T>C	ENSP00000339915.2:p.Phe1639Ser
ENST00000361917.5:c.4595T>C	ENSP00000355123.1:p.Phe1532Ser
ENST00000374708.8:c.4658T>C	ENSP00000363840.4:p.Phe1553Ser
ENST00000477772.1:n.706T>C
NM_080679.2:c.4595T>C	NP_542410.2:p.Phe1532Ser
NM_080680.2:c.4916T>C	NP_542411.2:p.Phe1639Ser
NM_080681.2:c.4658T>C	NP_542412.2:p.Phe1553Ser
XM_011514298.1:c.4070T>C	XP_011512600.1:p.Phe1357Ser
XM_011514299.1:c.4202T>C	XP_011512601.1:p.Phe1401Ser
XM_011514300.1:c.4022T>C	XP_011512602.1:p.Phe1341Ser
XM_011514301.1:c.3959T>C	XP_011512603.1:p.Phe1320Ser
XM_011514302.1:c.3803T>C	XP_011512604.1:p.Phe1268Ser
XM_011514299.2:c.4202T>C	XP_011512601.1:p.Phe1401Ser
XM_011514300.2:c.4022T>C	XP_011512602.1:p.Phe1341Ser
XM_011514302.2:c.3803T>C	XP_011512604.1:p.Phe1268Ser
XM_017010250.1:c.4916T>C	XP_016865739.1:p.Phe1639Ser
XM_017010251.2:c.3734T>C	XP_016865740.1:p.Phe1245Ser
NM_080680.3:c.4916T>C MANE Select	NP_542411.2:p.Phe1639Ser
NM_080681.3:c.4658T>C	NP_542412.2:p.Phe1553Ser
NM_080679.3:c.4595T>C	NP_542410.2:p.Phe1532Ser