Canonical Allele Identifier: CA2263917271
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50193027T= , CM000679.2:g.50193027T= GRCh38
NC_000017.10:g.48270388T= , CM000679.1:g.48270388T= GRCh37
NC_000017.9:g.45625387T= NCBI36
NG_007400.1:g.13613A= , LRG_1:g.13613A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1788A= MANE Select ENSP00000225964.6:p.Gly596=
ENST00000225964.9:c.1788A= ENSP00000225964.5:p.Gly596=
ENST00000476387.1:n.137A=
NM_000088.3:c.1788A= , LRG_1t1:c.1788A= NP_000079.2:p.Gly596=
XM_005257058.3:c.1788A= XP_005257115.2:p.Gly596=
XM_005257059.3:c.958-334A= XP_005257116.2:n.958-334A=
XM_011524341.1:c.1590A= XP_011522643.1:p.Gly530=
XM_005257058.4:c.1788A= XP_005257115.2:p.Gly596=
XM_005257059.4:c.958-334A= XP_005257116.2:n.958-334A=
NM_000088.4:c.1788A= MANE Select NP_000079.2:p.Gly596=