Canonical Allele Identifier: CA2263917802
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50193672G= , CM000679.2:g.50193672G= GRCh38
NC_000017.10:g.48271033G= , CM000679.1:g.48271033G= GRCh37
NC_000017.9:g.45626032G= NCBI36
NG_007400.1:g.12968C= , LRG_1:g.12968C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1767+271C= MANE Select ENSP00000225964.6:n.1767+271C=
ENST00000225964.9:c.1767+271C= ENSP00000225964.5:n.1767+271C=
ENST00000463440.1:n.428C=
ENST00000471344.1:n.1070C=
ENST00000476387.1:n.116+271C=
NM_000088.3:c.1767+271C= , LRG_1t1:c.1767+271C= NP_000079.2:n.1767+271C=
XM_005257058.3:c.1767+271C= XP_005257115.2:n.1767+271C=
XM_005257059.3:c.958-979C= XP_005257116.2:n.958-979C=
XM_011524341.1:c.1569+271C= XP_011522643.1:n.1569+271C=
XM_005257058.4:c.1767+271C= XP_005257115.2:n.1767+271C=
XM_005257059.4:c.958-979C= XP_005257116.2:n.958-979C=
NM_000088.4:c.1767+271C= MANE Select NP_000079.2:n.1767+271C=