Canonical Allele Identifier: CA2263913893
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185859G= , CM000679.2:g.50185859G= GRCh38
NC_000017.10:g.48263220G= , CM000679.1:g.48263220G= GRCh37
NC_000017.9:g.45618219G= NCBI36
NG_007400.1:g.20781C= , LRG_1:g.20781C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4167C= MANE Select ENSP00000225964.6:p.Leu1389=
ENST00000225964.9:c.4167C= ENSP00000225964.5:p.Leu1389=
ENST00000510710.3:n.1132C=
NM_000088.3:c.4167C= , LRG_1t1:c.4167C= NP_000079.2:p.Leu1389=
XM_005257058.3:c.3897C= XP_005257115.2:p.Leu1299=
XM_005257059.3:c.3249C= XP_005257116.2:p.Leu1083=
XM_011524341.1:c.3969C= XP_011522643.1:p.Leu1323=
XM_005257058.4:c.3897C= XP_005257115.2:p.Leu1299=
XM_005257059.4:c.3249C= XP_005257116.2:p.Leu1083=
NM_000088.4:c.4167C= MANE Select NP_000079.2:p.Leu1389=