Canonical Allele Identifier: CA2638703291
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185072_50185073insA , CM000679.2:g.50185072_50185073insA GRCh38
NC_000017.10:g.48262433_48262434insA , CM000679.1:g.48262433_48262434insA GRCh37
NC_000017.9:g.45617432_45617433insA NCBI36
NG_007400.1:g.21567_21568insT , LRG_1:g.21567_21568insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.*429_*430insT MANE Select ENSP00000225964.6:n.*429_*430insT
ENST00000225964.9:c.*429_*430insT ENSP00000225964.5:n.*429_*430insT
NM_000088.3:c.*429_*430insT , LRG_1t1:c.*429_*430insT NP_000079.2:n.*429_*430insT
XM_005257058.3:c.*429_*430insT XP_005257115.2:n.*429_*430insT
XM_005257059.3:c.*429_*430insT XP_005257116.2:n.*429_*430insT
XM_011524341.1:c.*429_*430insT XP_011522643.1:n.*429_*430insT
XM_005257058.4:c.*429_*430insT XP_005257115.2:n.*429_*430insT
XM_005257059.4:c.*429_*430insT XP_005257116.2:n.*429_*430insT
NM_000088.4:c.*429_*430insT MANE Select NP_000079.2:n.*429_*430insT