Canonical Allele Identifier: CA500850967
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48272952G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195591G>A , CM000679.2:g.50195591G>A GRCh38
NC_000017.10:g.48272952G>A , CM000679.1:g.48272952G>A GRCh37
NC_000017.9:g.45627951G>A NCBI36
NG_007400.1:g.11049C>T , LRG_1:g.11049C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1131C>T MANE Select ENSP00000225964.6:p.Gly377=
ENST00000225964.9:c.1131C>T ENSP00000225964.5:p.Gly377=
ENST00000471344.1:n.75C>T
NM_000088.3:c.1131C>T , LRG_1t1:c.1131C>T NP_000079.2:p.Gly377=
XM_005257058.3:c.1131C>T XP_005257115.2:p.Gly377=
XM_005257059.3:c.957+723C>T XP_005257116.2:n.957+723C>T
XM_011524341.1:c.958-113C>T XP_011522643.1:n.958-113C>T
XM_005257058.4:c.1131C>T XP_005257115.2:p.Gly377=
XM_005257059.4:c.957+723C>T XP_005257116.2:n.957+723C>T
NM_000088.4:c.1131C>T MANE Select NP_000079.2:p.Gly377=