Canonical Allele Identifier: CA363616637

Gene: COL11A2

Linked Data

• gnomAD v4: 6-33164463-A-G
• MyVariant Identifiers: chr6:g.33132240A>G (hg19) ; chr6:g.33164463A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164463A>G , CM000668.2:g.33164463A>G	GRCh38
NC_000006.11:g.33132240A>G , CM000668.1:g.33132240A>G	GRCh37
NC_000006.10:g.33240218A>G	NCBI36
NG_011589.1:g.33006T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.680T>C
ENST00000341947.7:c.4874T>C MANE Select	ENSP00000339915.2:p.Val1625Ala
ENST00000341947.6:c.4874T>C	ENSP00000339915.2:p.Val1625Ala
ENST00000361917.5:c.4553T>C	ENSP00000355123.1:p.Val1518Ala
ENST00000374708.8:c.4616T>C	ENSP00000363840.4:p.Val1539Ala
ENST00000477772.1:n.664T>C
NM_080679.2:c.4553T>C	NP_542410.2:p.Val1518Ala
NM_080680.2:c.4874T>C	NP_542411.2:p.Val1625Ala
NM_080681.2:c.4616T>C	NP_542412.2:p.Val1539Ala
XM_011514298.1:c.4028T>C	XP_011512600.1:p.Val1343Ala
XM_011514299.1:c.4160T>C	XP_011512601.1:p.Val1387Ala
XM_011514300.1:c.3980T>C	XP_011512602.1:p.Val1327Ala
XM_011514301.1:c.3917T>C	XP_011512603.1:p.Val1306Ala
XM_011514302.1:c.3761T>C	XP_011512604.1:p.Val1254Ala
XM_011514299.2:c.4160T>C	XP_011512601.1:p.Val1387Ala
XM_011514300.2:c.3980T>C	XP_011512602.1:p.Val1327Ala
XM_011514302.2:c.3761T>C	XP_011512604.1:p.Val1254Ala
XM_017010250.1:c.4874T>C	XP_016865739.1:p.Val1625Ala
XM_017010251.2:c.3692T>C	XP_016865740.1:p.Val1231Ala
NM_080680.3:c.4874T>C MANE Select	NP_542411.2:p.Val1625Ala
NM_080681.3:c.4616T>C	NP_542412.2:p.Val1539Ala
NM_080679.3:c.4553T>C	NP_542410.2:p.Val1518Ala