Canonical Allele Identifier: CA2263913729
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185590C= , CM000679.2:g.50185590C= GRCh38
NC_000017.10:g.48262951C= , CM000679.1:g.48262951C= GRCh37
NC_000017.9:g.45617950C= NCBI36
NG_007400.1:g.21050G= , LRG_1:g.21050G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4307G= MANE Select ENSP00000225964.6:p.Arg1436=
ENST00000225964.9:c.4307G= ENSP00000225964.5:p.Arg1436=
NM_000088.3:c.4307G= , LRG_1t1:c.4307G= NP_000079.2:p.Arg1436=
XM_005257058.3:c.4037G= XP_005257115.2:p.Arg1346=
XM_005257059.3:c.3389G= XP_005257116.2:p.Arg1130=
XM_011524341.1:c.4109G= XP_011522643.1:p.Arg1370=
XM_005257058.4:c.4037G= XP_005257115.2:p.Arg1346=
XM_005257059.4:c.3389G= XP_005257116.2:p.Arg1130=
NM_000088.4:c.4307G= MANE Select NP_000079.2:p.Arg1436=