Canonical Allele Identifier: CA2263913800
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185700G= , CM000679.2:g.50185700G= GRCh38
NC_000017.10:g.48263061G= , CM000679.1:g.48263061G= GRCh37
NC_000017.9:g.45618060G= NCBI36
NG_007400.1:g.20940C= , LRG_1:g.20940C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4249-52C= MANE Select ENSP00000225964.6:n.4249-52C=
ENST00000225964.9:c.4249-52C= ENSP00000225964.5:n.4249-52C=
NM_000088.3:c.4249-52C= , LRG_1t1:c.4249-52C= NP_000079.2:n.4249-52C=
XM_005257058.3:c.3979-52C= XP_005257115.2:n.3979-52C=
XM_005257059.3:c.3331-52C= XP_005257116.2:n.3331-52C=
XM_011524341.1:c.4051-52C= XP_011522643.1:n.4051-52C=
XM_005257058.4:c.3979-52C= XP_005257115.2:n.3979-52C=
XM_005257059.4:c.3331-52C= XP_005257116.2:n.3331-52C=
NM_000088.4:c.4249-52C= MANE Select NP_000079.2:n.4249-52C=