Canonical Allele Identifier: CA363617703

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132709C>G (hg19) ; chr6:g.33164932C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164932C>G , CM000668.2:g.33164932C>G	GRCh38
NC_000006.11:g.33132709C>G , CM000668.1:g.33132709C>G	GRCh37
NC_000006.10:g.33240687C>G	NCBI36
NG_011589.1:g.32537G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.589G>C
ENST00000341947.7:c.4783G>C MANE Select	ENSP00000339915.2:p.Ala1595Pro
ENST00000341947.6:c.4783G>C	ENSP00000339915.2:p.Ala1595Pro
ENST00000361917.5:c.4462G>C	ENSP00000355123.1:p.Ala1488Pro
ENST00000374708.8:c.4525G>C	ENSP00000363840.4:p.Ala1509Pro
ENST00000477772.1:n.573G>C
NM_080679.2:c.4462G>C	NP_542410.2:p.Ala1488Pro
NM_080680.2:c.4783G>C	NP_542411.2:p.Ala1595Pro
NM_080681.2:c.4525G>C	NP_542412.2:p.Ala1509Pro
XM_011514298.1:c.3937G>C	XP_011512600.1:p.Ala1313Pro
XM_011514299.1:c.4069G>C	XP_011512601.1:p.Ala1357Pro
XM_011514300.1:c.3889G>C	XP_011512602.1:p.Ala1297Pro
XM_011514301.1:c.3826G>C	XP_011512603.1:p.Ala1276Pro
XM_011514302.1:c.3670G>C	XP_011512604.1:p.Ala1224Pro
XM_011514299.2:c.4069G>C	XP_011512601.1:p.Ala1357Pro
XM_011514300.2:c.3889G>C	XP_011512602.1:p.Ala1297Pro
XM_011514302.2:c.3670G>C	XP_011512604.1:p.Ala1224Pro
XM_017010250.1:c.4783G>C	XP_016865739.1:p.Ala1595Pro
XM_017010251.2:c.3601G>C	XP_016865740.1:p.Ala1201Pro
NM_080680.3:c.4783G>C MANE Select	NP_542411.2:p.Ala1595Pro
NM_080681.3:c.4525G>C	NP_542412.2:p.Ala1509Pro
NM_080679.3:c.4462G>C	NP_542410.2:p.Ala1488Pro