Canonical Allele Identifier: CA2263918052
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194171T= , CM000679.2:g.50194171T= GRCh38
NC_000017.10:g.48271532T= , CM000679.1:g.48271532T= GRCh37
NC_000017.9:g.45626531T= NCBI36
NG_007400.1:g.12469A= , LRG_1:g.12469A=

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.1627A= MANE Select ENSP00000225964.6:p.Ser543=
ENST00000225964.9:c.1627A= ENSP00000225964.5:p.Ser543=
ENST00000463440.1:n.17A=
ENST00000471344.1:n.571A=
NM_000088.3:c.1627A= , LRG_1t1:c.1627A= NP_000079.2:p.Ser543=
XM_005257058.3:c.1627A= XP_005257115.2:p.Ser543=
XM_005257059.3:c.958-1478A= XP_005257116.2:n.958-1478A=
XM_011524341.1:c.1429A= XP_011522643.1:p.Ser477=
XM_005257058.4:c.1627A= XP_005257115.2:p.Ser543=
XM_005257059.4:c.958-1478A= XP_005257116.2:n.958-1478A=
NM_000088.4:c.1627A= MANE Select NP_000079.2:p.Ser543=