Canonical Allele Identifier: CA2263915188
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188531G= , CM000679.2:g.50188531G= GRCh38
NC_000017.10:g.48265892G= , CM000679.1:g.48265892G= GRCh37
NC_000017.9:g.45620891G= NCBI36
NG_007400.1:g.18109C= , LRG_1:g.18109C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.3206C= MANE Select ENSP00000225964.6:p.Thr1069=
ENST00000225964.9:c.3206C= ENSP00000225964.5:p.Thr1069=
ENST00000486572.1:n.24C=
ENST00000511732.1:n.150C=
NM_000088.3:c.3206C= , LRG_1t1:c.3206C= NP_000079.2:p.Thr1069=
XM_005257058.3:c.2936C= XP_005257115.2:p.Thr979=
XM_005257059.3:c.2288C= XP_005257116.2:p.Thr763=
XM_011524341.1:c.3008C= XP_011522643.1:p.Thr1003=
XM_005257058.4:c.2936C= XP_005257115.2:p.Thr979=
XM_005257059.4:c.2288C= XP_005257116.2:p.Thr763=
NM_000088.4:c.3206C= MANE Select NP_000079.2:p.Thr1069=