Canonical Allele Identifier: CA363617490

Gene: COL11A2

Linked Data

• gnomAD v4: 6-33164884-T-C
• MyVariant Identifiers: chr6:g.33132661T>C (hg19) ; chr6:g.33164884T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164884T>C , CM000668.2:g.33164884T>C	GRCh38
NC_000006.11:g.33132661T>C , CM000668.1:g.33132661T>C	GRCh37
NC_000006.10:g.33240639T>C	NCBI36
NG_011589.1:g.32585A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.637A>G
ENST00000341947.7:c.4831A>G MANE Select	ENSP00000339915.2:p.Thr1611Ala
ENST00000341947.6:c.4831A>G	ENSP00000339915.2:p.Thr1611Ala
ENST00000361917.5:c.4510A>G	ENSP00000355123.1:p.Thr1504Ala
ENST00000374708.8:c.4573A>G	ENSP00000363840.4:p.Thr1525Ala
ENST00000477772.1:n.621A>G
NM_080679.2:c.4510A>G	NP_542410.2:p.Thr1504Ala
NM_080680.2:c.4831A>G	NP_542411.2:p.Thr1611Ala
NM_080681.2:c.4573A>G	NP_542412.2:p.Thr1525Ala
XM_011514298.1:c.3985A>G	XP_011512600.1:p.Thr1329Ala
XM_011514299.1:c.4117A>G	XP_011512601.1:p.Thr1373Ala
XM_011514300.1:c.3937A>G	XP_011512602.1:p.Thr1313Ala
XM_011514301.1:c.3874A>G	XP_011512603.1:p.Thr1292Ala
XM_011514302.1:c.3718A>G	XP_011512604.1:p.Thr1240Ala
XM_011514299.2:c.4117A>G	XP_011512601.1:p.Thr1373Ala
XM_011514300.2:c.3937A>G	XP_011512602.1:p.Thr1313Ala
XM_011514302.2:c.3718A>G	XP_011512604.1:p.Thr1240Ala
XM_017010250.1:c.4831A>G	XP_016865739.1:p.Thr1611Ala
XM_017010251.2:c.3649A>G	XP_016865740.1:p.Thr1217Ala
NM_080680.3:c.4831A>G MANE Select	NP_542411.2:p.Thr1611Ala
NM_080681.3:c.4573A>G	NP_542412.2:p.Thr1525Ala
NM_080679.3:c.4510A>G	NP_542410.2:p.Thr1504Ala