Canonical Allele Identifier: CA363617406

Gene: COL11A2

Linked Data

• gnomAD v4: 6-33164863-C-A
• MyVariant Identifiers: chr6:g.33132640C>A (hg19) ; chr6:g.33164863C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164863C>A , CM000668.2:g.33164863C>A	GRCh38
NC_000006.11:g.33132640C>A , CM000668.1:g.33132640C>A	GRCh37
NC_000006.10:g.33240618C>A	NCBI36
NG_011589.1:g.32606G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000683572.1:n.658G>T
ENST00000341947.7:c.4852G>T MANE Select	ENSP00000339915.2:p.Asp1618Tyr
ENST00000341947.6:c.4852G>T	ENSP00000339915.2:p.Asp1618Tyr
ENST00000361917.5:c.4531G>T	ENSP00000355123.1:p.Asp1511Tyr
ENST00000374708.8:c.4594G>T	ENSP00000363840.4:p.Asp1532Tyr
ENST00000477772.1:n.642G>T
NM_080679.2:c.4531G>T	NP_542410.2:p.Asp1511Tyr
NM_080680.2:c.4852G>T	NP_542411.2:p.Asp1618Tyr
NM_080681.2:c.4594G>T	NP_542412.2:p.Asp1532Tyr
XM_011514298.1:c.4006G>T	XP_011512600.1:p.Asp1336Tyr
XM_011514299.1:c.4138G>T	XP_011512601.1:p.Asp1380Tyr
XM_011514300.1:c.3958G>T	XP_011512602.1:p.Asp1320Tyr
XM_011514301.1:c.3895G>T	XP_011512603.1:p.Asp1299Tyr
XM_011514302.1:c.3739G>T	XP_011512604.1:p.Asp1247Tyr
XM_011514299.2:c.4138G>T	XP_011512601.1:p.Asp1380Tyr
XM_011514300.2:c.3958G>T	XP_011512602.1:p.Asp1320Tyr
XM_011514302.2:c.3739G>T	XP_011512604.1:p.Asp1247Tyr
XM_017010250.1:c.4852G>T	XP_016865739.1:p.Asp1618Tyr
XM_017010251.2:c.3670G>T	XP_016865740.1:p.Asp1224Tyr
NM_080680.3:c.4852G>T MANE Select	NP_542411.2:p.Asp1618Tyr
NM_080681.3:c.4594G>T	NP_542412.2:p.Asp1532Tyr
NM_080679.3:c.4531G>T	NP_542410.2:p.Asp1511Tyr