Canonical Allele Identifier: CA2263920587
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199229T= , CM000679.2:g.50199229T= GRCh38
NC_000017.10:g.48276590T= , CM000679.1:g.48276590T= GRCh37
NC_000017.9:g.45631589T= NCBI36
NG_007400.1:g.7411A= , LRG_1:g.7411A=

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.468A= MANE Select ENSP00000225964.6:p.Gly156=
ENST00000225964.9:c.468A= ENSP00000225964.5:p.Gly156=
NM_000088.3:c.468A= , LRG_1t1:c.468A= NP_000079.2:p.Gly156=
XM_005257058.3:c.468A= XP_005257115.2:p.Gly156=
XM_005257059.3:c.468A= XP_005257116.2:p.Gly156=
XM_011524341.1:c.468A= XP_011522643.1:p.Gly156=
XM_005257058.4:c.468A= XP_005257115.2:p.Gly156=
XM_005257059.4:c.468A= XP_005257116.2:p.Gly156=
NM_000088.4:c.468A= MANE Select NP_000079.2:p.Gly156=