Canonical Allele Identifier: CA363617812

Gene: COL11A2

Linked Data

• gnomAD v4: 6-33164947-G-T
• COSMIC: COSM4949978
• MyVariant Identifiers: chr6:g.33132724G>T (hg19) ; chr6:g.33164947G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164947G>T , CM000668.2:g.33164947G>T	GRCh38
NC_000006.11:g.33132724G>T , CM000668.1:g.33132724G>T	GRCh37
NC_000006.10:g.33240702G>T	NCBI36
NG_011589.1:g.32522C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.574C>A
ENST00000341947.7:c.4768C>A MANE Select	ENSP00000339915.2:p.Pro1590Thr
ENST00000341947.6:c.4768C>A	ENSP00000339915.2:p.Pro1590Thr
ENST00000361917.5:c.4447C>A	ENSP00000355123.1:p.Pro1483Thr
ENST00000374708.8:c.4510C>A	ENSP00000363840.4:p.Pro1504Thr
ENST00000477772.1:n.558C>A
NM_080679.2:c.4447C>A	NP_542410.2:p.Pro1483Thr
NM_080680.2:c.4768C>A	NP_542411.2:p.Pro1590Thr
NM_080681.2:c.4510C>A	NP_542412.2:p.Pro1504Thr
XM_011514298.1:c.3922C>A	XP_011512600.1:p.Pro1308Thr
XM_011514299.1:c.4054C>A	XP_011512601.1:p.Pro1352Thr
XM_011514300.1:c.3874C>A	XP_011512602.1:p.Pro1292Thr
XM_011514301.1:c.3811C>A	XP_011512603.1:p.Pro1271Thr
XM_011514302.1:c.3655C>A	XP_011512604.1:p.Pro1219Thr
XM_011514299.2:c.4054C>A	XP_011512601.1:p.Pro1352Thr
XM_011514300.2:c.3874C>A	XP_011512602.1:p.Pro1292Thr
XM_011514302.2:c.3655C>A	XP_011512604.1:p.Pro1219Thr
XM_017010250.1:c.4768C>A	XP_016865739.1:p.Pro1590Thr
XM_017010251.2:c.3586C>A	XP_016865740.1:p.Pro1196Thr
NM_080680.3:c.4768C>A MANE Select	NP_542411.2:p.Pro1590Thr
NM_080681.3:c.4510C>A	NP_542412.2:p.Pro1504Thr
NM_080679.3:c.4447C>A	NP_542410.2:p.Pro1483Thr