Canonical Allele Identifier: CA2263913640
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185457_50185458delinsGA , CM000679.2:g.50185457_50185458delinsGA GRCh38
NC_000017.10:g.48262818_48262819delinsGA , CM000679.1:g.48262818_48262819delinsGA GRCh37
NC_000017.9:g.45617817_45617818delinsGA NCBI36
NG_007400.1:g.21182_21183delinsTC , LRG_1:g.21182_21183delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.*44_*45delinsTC MANE Select ENSP00000225964.6:n.*44_*45delinsTC
ENST00000225964.9:c.*44_*45delinsTC ENSP00000225964.5:n.*44_*45delinsTC
NM_000088.3:c.*44_*45delinsTC , LRG_1t1:c.*44_*45delinsTC NP_000079.2:n.*44_*45delinsTC
XM_005257058.3:c.*44_*45delinsTC XP_005257115.2:n.*44_*45delinsTC
XM_005257059.3:c.*44_*45delinsTC XP_005257116.2:n.*44_*45delinsTC
XM_011524341.1:c.*44_*45delinsTC XP_011522643.1:n.*44_*45delinsTC
XM_005257058.4:c.*44_*45delinsTC XP_005257115.2:n.*44_*45delinsTC
XM_005257059.4:c.*44_*45delinsTC XP_005257116.2:n.*44_*45delinsTC
NM_000088.4:c.*44_*45delinsTC MANE Select NP_000079.2:n.*44_*45delinsTC