Canonical Allele Identifier: CA1726750329
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409209_94409210delinsTA , CM000669.2:g.94409209_94409210delinsTA GRCh38
NC_000007.13:g.94038521_94038522delinsTA , CM000669.1:g.94038521_94038522delinsTA GRCh37
NC_000007.12:g.93876457_93876458delinsTA NCBI36
NG_007405.1:g.19649_19650delinsTA , LRG_2:g.19649_19650delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.793-113_793-112delinsTA MANE Select ENSP00000297268.6:n.793-113_793-112delinsTA
ENST00000297268.10:c.793-113_793-112delinsTA ENSP00000297268.6:n.793-113_793-112delinsTA
ENST00000620463.1:c.787-113_787-112delinsTA ENSP00000477719.1:n.787-113_787-112delinsTA
NM_000089.3:c.793-113_793-112delinsTA , LRG_2t1:c.793-113_793-112delinsTA NP_000080.2:n.793-113_793-112delinsTA
NM_000089.4:c.793-113_793-112delinsTA MANE Select NP_000080.2:n.793-113_793-112delinsTA