Canonical Allele Identifier: CA2263913788
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185687C= , CM000679.2:g.50185687C= GRCh38
NC_000017.10:g.48263048C= , CM000679.1:g.48263048C= GRCh37
NC_000017.9:g.45618047C= NCBI36
NG_007400.1:g.20953G= , LRG_1:g.20953G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4249-39G= MANE Select ENSP00000225964.6:n.4249-39G=
ENST00000225964.9:c.4249-39G= ENSP00000225964.5:n.4249-39G=
NM_000088.3:c.4249-39G= , LRG_1t1:c.4249-39G= NP_000079.2:n.4249-39G=
XM_005257058.3:c.3979-39G= XP_005257115.2:n.3979-39G=
XM_005257059.3:c.3331-39G= XP_005257116.2:n.3331-39G=
XM_011524341.1:c.4051-39G= XP_011522643.1:n.4051-39G=
XM_005257058.4:c.3979-39G= XP_005257115.2:n.3979-39G=
XM_005257059.4:c.3331-39G= XP_005257116.2:n.3331-39G=
NM_000088.4:c.4249-39G= MANE Select NP_000079.2:n.4249-39G=