Canonical Allele Identifier: CA2263918379
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194768G= , CM000679.2:g.50194768G= GRCh38
NC_000017.10:g.48272129G= , CM000679.1:g.48272129G= GRCh37
NC_000017.9:g.45627128G= NCBI36
NG_007400.1:g.11872C= , LRG_1:g.11872C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1414C= MANE Select ENSP00000225964.6:p.Arg472=
ENST00000225964.9:c.1414C= ENSP00000225964.5:p.Arg472=
ENST00000471344.1:n.358C=
NM_000088.3:c.1414C= , LRG_1t1:c.1414C= NP_000079.2:p.Arg472=
XM_005257058.3:c.1414C= XP_005257115.2:p.Arg472=
XM_005257059.3:c.957+1546C= XP_005257116.2:n.957+1546C=
XM_011524341.1:c.1216C= XP_011522643.1:p.Arg406=
XM_005257058.4:c.1414C= XP_005257115.2:p.Arg472=
XM_005257059.4:c.957+1546C= XP_005257116.2:n.957+1546C=
NM_000088.4:c.1414C= MANE Select NP_000079.2:p.Arg472=