Canonical Allele Identifier: CA2263915162
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188492C= , CM000679.2:g.50188492C= GRCh38
NC_000017.10:g.48265853C= , CM000679.1:g.48265853C= GRCh37
NC_000017.9:g.45620852C= NCBI36
NG_007400.1:g.18148G= , LRG_1:g.18148G=

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.3207+38G= MANE Select ENSP00000225964.6:n.3207+38G=
ENST00000225964.9:c.3207+38G= ENSP00000225964.5:n.3207+38G=
ENST00000486572.1:n.63G=
ENST00000511732.1:n.189G=
NM_000088.3:c.3207+38G= , LRG_1t1:c.3207+38G= NP_000079.2:n.3207+38G=
XM_005257058.3:c.2937+38G= XP_005257115.2:n.2937+38G=
XM_005257059.3:c.2289+38G= XP_005257116.2:n.2289+38G=
XM_011524341.1:c.3009+38G= XP_011522643.1:n.3009+38G=
XM_005257058.4:c.2937+38G= XP_005257115.2:n.2937+38G=
XM_005257059.4:c.2289+38G= XP_005257116.2:n.2289+38G=
NM_000088.4:c.3207+38G= MANE Select NP_000079.2:n.3207+38G=