Canonical Allele Identifier: CA2263915138
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188445T= , CM000679.2:g.50188445T= GRCh38
NC_000017.10:g.48265806T= , CM000679.1:g.48265806T= GRCh37
NC_000017.9:g.45620805T= NCBI36
NG_007400.1:g.18195A= , LRG_1:g.18195A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.3207+85A= MANE Select ENSP00000225964.6:n.3207+85A=
ENST00000225964.9:c.3207+85A= ENSP00000225964.5:n.3207+85A=
ENST00000486572.1:n.110A=
ENST00000511732.1:n.236A=
NM_000088.3:c.3207+85A= , LRG_1t1:c.3207+85A= NP_000079.2:n.3207+85A=
XM_005257058.3:c.2937+85A= XP_005257115.2:n.2937+85A=
XM_005257059.3:c.2289+85A= XP_005257116.2:n.2289+85A=
XM_011524341.1:c.3009+85A= XP_011522643.1:n.3009+85A=
XM_005257058.4:c.2937+85A= XP_005257115.2:n.2937+85A=
XM_005257059.4:c.2289+85A= XP_005257116.2:n.2289+85A=
NM_000088.4:c.3207+85A= MANE Select NP_000079.2:n.3207+85A=