Canonical Allele Identifier: CA772790277
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1323503514

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50193259del , CM000679.2:g.50193259del GRCh38
NC_000017.10:g.48270620del , CM000679.1:g.48270620del GRCh37
NC_000017.9:g.45625619del NCBI36
NG_007400.1:g.13383del , LRG_1:g.13383del

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1768-210del MANE Select ENSP00000225964.6:n.1768-210del
ENST00000225964.9:c.1768-210del ENSP00000225964.5:n.1768-210del
ENST00000476387.1:n.117-210del
NM_000088.3:c.1768-210del , LRG_1t1:c.1768-210del NP_000079.2:n.1768-210del
XM_005257058.3:c.1768-210del XP_005257115.2:n.1768-210del
XM_005257059.3:c.958-564del XP_005257116.2:n.958-564del
XM_011524341.1:c.1570-210del XP_011522643.1:n.1570-210del
XM_005257058.4:c.1768-210del XP_005257115.2:n.1768-210del
XM_005257059.4:c.958-564del XP_005257116.2:n.958-564del
NM_000088.4:c.1768-210del MANE Select NP_000079.2:n.1768-210del