Canonical Allele Identifier: CA1726763440
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94415266C= , CM000669.2:g.94415266C= GRCh38
NC_000007.13:g.94044578C= , CM000669.1:g.94044578C= GRCh37
NC_000007.12:g.93882514C= NCBI36
NG_007405.1:g.25706C= , LRG_2:g.25706C=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.1760C= MANE Select ENSP00000297268.6:p.Pro587=
ENST00000297268.10:c.1760C= ENSP00000297268.6:p.Pro587=
ENST00000473573.5:n.97C=
ENST00000488298.5:n.184C=
ENST00000620463.1:c.1754C= ENSP00000477719.1:p.Pro585=
NM_000089.3:c.1760C= , LRG_2t1:c.1760C= NP_000080.2:p.Pro587=
NM_000089.4:c.1760C= MANE Select NP_000080.2:p.Pro587=