Canonical Allele Identifier: CA2263913920
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185912T= , CM000679.2:g.50185912T= GRCh38
NC_000017.10:g.48263273T= , CM000679.1:g.48263273T= GRCh37
NC_000017.9:g.45618272T= NCBI36
NG_007400.1:g.20728A= , LRG_1:g.20728A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4114A= MANE Select ENSP00000225964.6:p.Asn1372=
ENST00000225964.9:c.4114A= ENSP00000225964.5:p.Asn1372=
ENST00000510710.3:n.1079A=
NM_000088.3:c.4114A= , LRG_1t1:c.4114A= NP_000079.2:p.Asn1372=
XM_005257058.3:c.3844A= XP_005257115.2:p.Asn1282=
XM_005257059.3:c.3196A= XP_005257116.2:p.Asn1066=
XM_011524341.1:c.3916A= XP_011522643.1:p.Asn1306=
XM_005257058.4:c.3844A= XP_005257115.2:p.Asn1282=
XM_005257059.4:c.3196A= XP_005257116.2:p.Asn1066=
NM_000088.4:c.4114A= MANE Select NP_000079.2:p.Asn1372=