Canonical Allele Identifier: CA449867310

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132701A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164924A>G , CM000668.2:g.33164924A>G	GRCh38
NC_000006.11:g.33132701A>G , CM000668.1:g.33132701A>G	GRCh37
NC_000006.10:g.33240679A>G	NCBI36
NG_011589.1:g.32545T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.597T>C
ENST00000341947.7:c.4791T>C MANE Select	ENSP00000339915.2:p.Asp1597=
ENST00000341947.6:c.4791T>C	ENSP00000339915.2:p.Asp1597=
ENST00000361917.5:c.4470T>C	ENSP00000355123.1:p.Asp1490=
ENST00000374708.8:c.4533T>C	ENSP00000363840.4:p.Asp1511=
ENST00000477772.1:n.581T>C
NM_080679.2:c.4470T>C	NP_542410.2:p.Asp1490=
NM_080680.2:c.4791T>C	NP_542411.2:p.Asp1597=
NM_080681.2:c.4533T>C	NP_542412.2:p.Asp1511=
XM_011514298.1:c.3945T>C	XP_011512600.1:p.Asp1315=
XM_011514299.1:c.4077T>C	XP_011512601.1:p.Asp1359=
XM_011514300.1:c.3897T>C	XP_011512602.1:p.Asp1299=
XM_011514301.1:c.3834T>C	XP_011512603.1:p.Asp1278=
XM_011514302.1:c.3678T>C	XP_011512604.1:p.Asp1226=
XM_011514299.2:c.4077T>C	XP_011512601.1:p.Asp1359=
XM_011514300.2:c.3897T>C	XP_011512602.1:p.Asp1299=
XM_011514302.2:c.3678T>C	XP_011512604.1:p.Asp1226=
XM_017010250.1:c.4791T>C	XP_016865739.1:p.Asp1597=
XM_017010251.2:c.3609T>C	XP_016865740.1:p.Asp1203=
NM_080680.3:c.4791T>C MANE Select	NP_542411.2:p.Asp1597=
NM_080681.3:c.4533T>C	NP_542412.2:p.Asp1511=
NM_080679.3:c.4470T>C	NP_542410.2:p.Asp1490=