Canonical Allele Identifier: CA363616524

Gene: COL11A2

Linked Data

• gnomAD v4: 6-33164437-C-T
• MyVariant Identifiers: chr6:g.33132214C>T (hg19) ; chr6:g.33164437C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164437C>T , CM000668.2:g.33164437C>T	GRCh38
NC_000006.11:g.33132214C>T , CM000668.1:g.33132214C>T	GRCh37
NC_000006.10:g.33240192C>T	NCBI36
NG_011589.1:g.33032G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.706G>A
ENST00000341947.7:c.4900G>A MANE Select	ENSP00000339915.2:p.Val1634Met
ENST00000341947.6:c.4900G>A	ENSP00000339915.2:p.Val1634Met
ENST00000361917.5:c.4579G>A	ENSP00000355123.1:p.Val1527Met
ENST00000374708.8:c.4642G>A	ENSP00000363840.4:p.Val1548Met
ENST00000477772.1:n.690G>A
NM_080679.2:c.4579G>A	NP_542410.2:p.Val1527Met
NM_080680.2:c.4900G>A	NP_542411.2:p.Val1634Met
NM_080681.2:c.4642G>A	NP_542412.2:p.Val1548Met
XM_011514298.1:c.4054G>A	XP_011512600.1:p.Val1352Met
XM_011514299.1:c.4186G>A	XP_011512601.1:p.Val1396Met
XM_011514300.1:c.4006G>A	XP_011512602.1:p.Val1336Met
XM_011514301.1:c.3943G>A	XP_011512603.1:p.Val1315Met
XM_011514302.1:c.3787G>A	XP_011512604.1:p.Val1263Met
XM_011514299.2:c.4186G>A	XP_011512601.1:p.Val1396Met
XM_011514300.2:c.4006G>A	XP_011512602.1:p.Val1336Met
XM_011514302.2:c.3787G>A	XP_011512604.1:p.Val1263Met
XM_017010250.1:c.4900G>A	XP_016865739.1:p.Val1634Met
XM_017010251.2:c.3718G>A	XP_016865740.1:p.Val1240Met
NM_080680.3:c.4900G>A MANE Select	NP_542411.2:p.Val1634Met
NM_080681.3:c.4642G>A	NP_542412.2:p.Val1548Met
NM_080679.3:c.4579G>A	NP_542410.2:p.Val1527Met