Canonical Allele Identifier: CA2263918680
Community Standard Title: NM_000088.4(COL1A1):c.1235C= (p.Pro412=)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195296G= , CM000679.2:g.50195296G= GRCh38
NC_000017.10:g.48272657G= , CM000679.1:g.48272657G= GRCh37
NC_000017.9:g.45627656G= NCBI36
NG_007400.1:g.11344C= , LRG_1:g.11344C=

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.1235C= MANE Select NP_000079.2:p.Pro412=
ENST00000225964.10:c.1235C= MANE Select ENSP00000225964.6:p.Pro412=
NM_000088.3:c.1235C= , LRG_1t1:c.1235C= NP_000079.2:p.Pro412=
ENST00000225964.9:c.1235C= ENSP00000225964.5:p.Pro412=
ENST00000471344.1:n.179C=
XM_005257058.3:c.1235C= XP_005257115.2:p.Pro412=
XM_005257058.4:c.1235C= XP_005257115.2:p.Pro412=
XM_005257059.3:c.957+1018C= XP_005257116.2:n.957+1018C=
XM_005257059.4:c.957+1018C= XP_005257116.2:n.957+1018C=
XM_011524341.1:c.1037C= XP_011522643.1:p.Pro346=