Canonical Allele Identifier: CA2263914940
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188035G= , CM000679.2:g.50188035G= GRCh38
NC_000017.10:g.48265396G= , CM000679.1:g.48265396G= GRCh37
NC_000017.9:g.45620395G= NCBI36
NG_007400.1:g.18605C= , LRG_1:g.18605C=

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.3262-52C= MANE Select ENSP00000225964.6:n.3262-52C=
ENST00000225964.9:c.3262-52C= ENSP00000225964.5:n.3262-52C=
ENST00000486572.1:n.460-52C=
ENST00000511732.1:n.646C=
NM_000088.3:c.3262-52C= , LRG_1t1:c.3262-52C= NP_000079.2:n.3262-52C=
XM_005257058.3:c.2992-52C= XP_005257115.2:n.2992-52C=
XM_005257059.3:c.2344-52C= XP_005257116.2:n.2344-52C=
XM_011524341.1:c.3064-52C= XP_011522643.1:n.3064-52C=
XM_005257058.4:c.2992-52C= XP_005257115.2:n.2992-52C=
XM_005257059.4:c.2344-52C= XP_005257116.2:n.2344-52C=
NM_000088.4:c.3262-52C= MANE Select NP_000079.2:n.3262-52C=