Canonical Allele Identifier: CA2683766780
Gene: COL1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401528_94401529insA , CM000669.2:g.94401528_94401529insA GRCh38
NC_000007.13:g.94030840_94030841insA , CM000669.1:g.94030840_94030841insA GRCh37
NC_000007.12:g.93868776_93868777insA NCBI36
NG_007405.1:g.11968_11969insA , LRG_2:g.11968_11969insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.226-39_226-38insA MANE Select ENSP00000297268.6:n.226-39_226-38insA
ENST00000297268.10:c.226-39_226-38insA ENSP00000297268.6:n.226-39_226-38insA
ENST00000620463.1:c.220-39_220-38insA ENSP00000477719.1:n.220-39_220-38insA
NM_000089.3:c.226-39_226-38insA , LRG_2t1:c.226-39_226-38insA NP_000080.2:n.226-39_226-38insA
NM_000089.4:c.226-39_226-38insA MANE Select NP_000080.2:n.226-39_226-38insA