Canonical Allele Identifier: CA2678231771

Gene: COL11A2

Linked Data

• gnomAD v4: 6-33192341-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33192341G>T , CM000668.2:g.33192341G>T	GRCh38
NC_000006.11:g.33160118G>T , CM000668.1:g.33160118G>T	GRCh37
NC_000006.10:g.33268096G>T	NCBI36
NG_011589.1:g.5128C>A
NG_023374.1:g.13315C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341947.7:c.-101C>A MANE Select	ENSP00000339915.2:n.-101C>A
ENST00000341947.6:c.-101C>A	ENSP00000339915.2:n.-101C>A
ENST00000361917.5:c.-101C>A	ENSP00000355123.1:n.-101C>A
ENST00000374708.8:c.-101C>A	ENSP00000363840.4:n.-101C>A
ENST00000395194.1:c.-101C>A	ENSP00000378620.1:n.-101C>A
ENST00000457788.5:c.-101C>A	ENSP00000405520.1:n.-101C>A
NM_001163771.1:c.-101C>A	NP_001157243.1:n.-101C>A
NM_080679.2:c.-101C>A	NP_542410.2:n.-101C>A
NM_080680.2:c.-101C>A	NP_542411.2:n.-101C>A
NM_080681.2:c.-101C>A	NP_542412.2:n.-101C>A
XM_011514298.1:c.-765+684C>A	XP_011512600.1:n.-765+684C>A
XM_017010250.1:c.-66-35C>A	XP_016865739.1:n.-66-35C>A
NM_001163771.2:c.-101C>A	NP_001157243.1:n.-101C>A
NM_080680.3:c.-101C>A MANE Select	NP_542411.2:n.-101C>A
NM_080681.3:c.-101C>A	NP_542412.2:n.-101C>A
NM_080679.3:c.-101C>A	NP_542410.2:n.-101C>A