Canonical Allele Identifier: CA2263918327
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194690G= , CM000679.2:g.50194690G= GRCh38
NC_000017.10:g.48272051G= , CM000679.1:g.48272051G= GRCh37
NC_000017.9:g.45627050G= NCBI36
NG_007400.1:g.11950C= , LRG_1:g.11950C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1461+31C= MANE Select ENSP00000225964.6:n.1461+31C=
ENST00000225964.9:c.1461+31C= ENSP00000225964.5:n.1461+31C=
ENST00000471344.1:n.405+31C=
NM_000088.3:c.1461+31C= , LRG_1t1:c.1461+31C= NP_000079.2:n.1461+31C=
XM_005257058.3:c.1461+31C= XP_005257115.2:n.1461+31C=
XM_005257059.3:c.957+1624C= XP_005257116.2:n.957+1624C=
XM_011524341.1:c.1263+31C= XP_011522643.1:n.1263+31C=
XM_005257058.4:c.1461+31C= XP_005257115.2:n.1461+31C=
XM_005257059.4:c.957+1624C= XP_005257116.2:n.957+1624C=
NM_000088.4:c.1461+31C= MANE Select NP_000079.2:n.1461+31C=