Canonical Allele Identifier: CA2678217247

Gene: COL11A2

Linked Data

• gnomAD v4: 6-33174441-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33174441G>A , CM000668.2:g.33174441G>A	GRCh38
NC_000006.11:g.33142218G>A , CM000668.1:g.33142218G>A	GRCh37
NC_000006.10:g.33250196G>A	NCBI36
NG_011589.1:g.23028C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000361917.6:c.1003+86C>T
ENST00000341947.7:c.2430+86C>T MANE Select	ENSP00000339915.2:n.2430+86C>T
ENST00000341947.6:c.2430+86C>T	ENSP00000339915.2:n.2430+86C>T
ENST00000361917.5:c.2109+86C>T	ENSP00000355123.1:n.2109+86C>T
ENST00000374708.8:c.2172+86C>T	ENSP00000363840.4:n.2172+86C>T
ENST00000477772.1:n.272+2568C>T
NM_080679.2:c.2109+86C>T	NP_542410.2:n.2109+86C>T
NM_080680.2:c.2430+86C>T	NP_542411.2:n.2430+86C>T
NM_080681.2:c.2172+86C>T	NP_542412.2:n.2172+86C>T
XM_011514298.1:c.1584+86C>T	XP_011512600.1:n.1584+86C>T
XM_011514299.1:c.1716+86C>T	XP_011512601.1:n.1716+86C>T
XM_011514300.1:c.1536+86C>T	XP_011512602.1:n.1536+86C>T
XM_011514301.1:c.1473+86C>T	XP_011512603.1:n.1473+86C>T
XM_011514302.1:c.1317+86C>T	XP_011512604.1:n.1317+86C>T
XM_011514299.2:c.1716+86C>T	XP_011512601.1:n.1716+86C>T
XM_011514300.2:c.1536+86C>T	XP_011512602.1:n.1536+86C>T
XM_011514302.2:c.1317+86C>T	XP_011512604.1:n.1317+86C>T
XM_017010250.1:c.2430+86C>T	XP_016865739.1:n.2430+86C>T
XM_017010251.2:c.1248+86C>T	XP_016865740.1:n.1248+86C>T
NM_080680.3:c.2430+86C>T MANE Select	NP_542411.2:n.2430+86C>T
NM_080681.3:c.2172+86C>T	NP_542412.2:n.2172+86C>T
NM_080679.3:c.2109+86C>T	NP_542410.2:n.2109+86C>T