Canonical Allele Identifier: CA2263913895
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185863A= , CM000679.2:g.50185863A= GRCh38
NC_000017.10:g.48263224A= , CM000679.1:g.48263224A= GRCh37
NC_000017.9:g.45618223A= NCBI36
NG_007400.1:g.20777T= , LRG_1:g.20777T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4163T= MANE Select ENSP00000225964.6:p.Leu1388=
ENST00000225964.9:c.4163T= ENSP00000225964.5:p.Leu1388=
ENST00000510710.3:n.1128T=
NM_000088.3:c.4163T= , LRG_1t1:c.4163T= NP_000079.2:p.Leu1388=
XM_005257058.3:c.3893T= XP_005257115.2:p.Leu1298=
XM_005257059.3:c.3245T= XP_005257116.2:p.Leu1082=
XM_011524341.1:c.3965T= XP_011522643.1:p.Leu1322=
XM_005257058.4:c.3893T= XP_005257115.2:p.Leu1298=
XM_005257059.4:c.3245T= XP_005257116.2:p.Leu1082=
NM_000088.4:c.4163T= MANE Select NP_000079.2:p.Leu1388=