Canonical Allele Identifier: CA772790234
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1317674838

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50193183del , CM000679.2:g.50193183del GRCh38
NC_000017.10:g.48270544del , CM000679.1:g.48270544del GRCh37
NC_000017.9:g.45625543del NCBI36
NG_007400.1:g.13460del , LRG_1:g.13460del

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1768-133del MANE Select ENSP00000225964.6:n.1768-133del
ENST00000225964.9:c.1768-133del ENSP00000225964.5:n.1768-133del
ENST00000476387.1:n.117-133del
NM_000088.3:c.1768-133del , LRG_1t1:c.1768-133del NP_000079.2:n.1768-133del
XM_005257058.3:c.1768-133del XP_005257115.2:n.1768-133del
XM_005257059.3:c.958-487del XP_005257116.2:n.958-487del
XM_011524341.1:c.1570-133del XP_011522643.1:n.1570-133del
XM_005257058.4:c.1768-133del XP_005257115.2:n.1768-133del
XM_005257059.4:c.958-487del XP_005257116.2:n.958-487del
NM_000088.4:c.1768-133del MANE Select NP_000079.2:n.1768-133del