Canonical Allele Identifier: CA2263918992
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195941_50195942delinsAG , CM000679.2:g.50195941_50195942delinsAG GRCh38
NC_000017.10:g.48273302_48273303delinsAG , CM000679.1:g.48273302_48273303delinsAG GRCh37
NC_000017.9:g.45628301_45628302delinsAG NCBI36
NG_007400.1:g.10698_10699delinsCT , LRG_1:g.10698_10699delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.1037_1038delinsCT MANE Select ENSP00000225964.6:p.Pro346=
ENST00000225964.9:c.1037_1038delinsCT ENSP00000225964.5:p.Pro346=
NM_000088.3:c.1037_1038delinsCT , LRG_1t1:c.1037_1038delinsCT NP_000079.2:p.Pro346=
XM_005257058.3:c.1037_1038delinsCT XP_005257115.2:p.Pro346=
XM_005257059.3:c.957+372_957+373delinsCT XP_005257116.2:n.957+372_957+373delinsCT
XM_011524341.1:c.957+372_957+373delinsCT XP_011522643.1:n.957+372_957+373delinsCT
XM_005257058.4:c.1037_1038delinsCT XP_005257115.2:p.Pro346=
XM_005257059.4:c.957+372_957+373delinsCT XP_005257116.2:n.957+372_957+373delinsCT
NM_000088.4:c.1037_1038delinsCT MANE Select NP_000079.2:p.Pro346=