Canonical Allele Identifier: CA1726783432
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426586_94426588delinsGAA , CM000669.2:g.94426586_94426588delinsGAA GRCh38
NC_000007.13:g.94055898_94055900delinsGAA , CM000669.1:g.94055898_94055900delinsGAA GRCh37
NC_000007.12:g.93893834_93893836delinsGAA NCBI36
NG_007405.1:g.37026_37028delinsGAA , LRG_2:g.37026_37028delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.3105+56_3105+58delinsGAA MANE Select ENSP00000297268.6:n.3105+56_3105+58delinsGAA
ENST00000297268.10:c.3105+56_3105+58delinsGAA ENSP00000297268.6:n.3105+56_3105+58delinsGAA
ENST00000478215.1:n.720_722delinsGAA
ENST00000481570.5:n.3134_3136delinsGAA
ENST00000488121.1:n.21+56_21+58delinsGAA
ENST00000620463.1:c.3099+56_3099+58delinsGAA ENSP00000477719.1:n.3099+56_3099+58delinsGAA
NM_000089.3:c.3105+56_3105+58delinsGAA , LRG_2t1:c.3105+56_3105+58delinsGAA NP_000080.2:n.3105+56_3105+58delinsGAA
NM_000089.4:c.3105+56_3105+58delinsGAA MANE Select NP_000080.2:n.3105+56_3105+58delinsGAA