Canonical Allele Identifier: CA449867298

Gene: COL11A2

Linked Data

• gnomAD v4: 6-33164909-G-A
• MyVariant Identifiers: chr6:g.33132686G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164909G>A , CM000668.2:g.33164909G>A	GRCh38
NC_000006.11:g.33132686G>A , CM000668.1:g.33132686G>A	GRCh37
NC_000006.10:g.33240664G>A	NCBI36
NG_011589.1:g.32560C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.612C>T
ENST00000341947.7:c.4806C>T MANE Select	ENSP00000339915.2:p.Phe1602=
ENST00000341947.6:c.4806C>T	ENSP00000339915.2:p.Phe1602=
ENST00000361917.5:c.4485C>T	ENSP00000355123.1:p.Phe1495=
ENST00000374708.8:c.4548C>T	ENSP00000363840.4:p.Phe1516=
ENST00000477772.1:n.596C>T
NM_080679.2:c.4485C>T	NP_542410.2:p.Phe1495=
NM_080680.2:c.4806C>T	NP_542411.2:p.Phe1602=
NM_080681.2:c.4548C>T	NP_542412.2:p.Phe1516=
XM_011514298.1:c.3960C>T	XP_011512600.1:p.Phe1320=
XM_011514299.1:c.4092C>T	XP_011512601.1:p.Phe1364=
XM_011514300.1:c.3912C>T	XP_011512602.1:p.Phe1304=
XM_011514301.1:c.3849C>T	XP_011512603.1:p.Phe1283=
XM_011514302.1:c.3693C>T	XP_011512604.1:p.Phe1231=
XM_011514299.2:c.4092C>T	XP_011512601.1:p.Phe1364=
XM_011514300.2:c.3912C>T	XP_011512602.1:p.Phe1304=
XM_011514302.2:c.3693C>T	XP_011512604.1:p.Phe1231=
XM_017010250.1:c.4806C>T	XP_016865739.1:p.Phe1602=
XM_017010251.2:c.3624C>T	XP_016865740.1:p.Phe1208=
NM_080680.3:c.4806C>T MANE Select	NP_542411.2:p.Phe1602=
NM_080681.3:c.4548C>T	NP_542412.2:p.Phe1516=
NM_080679.3:c.4485C>T	NP_542410.2:p.Phe1495=