Canonical Allele Identifier: CA500991408
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185595G>A , CM000679.2:g.50185595G>A GRCh38
NC_000017.10:g.48262956G>A , CM000679.1:g.48262956G>A GRCh37
NC_000017.9:g.45617955G>A NCBI36
NG_007400.1:g.21045C>T , LRG_1:g.21045C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4302C>T MANE Select ENSP00000225964.6:p.Thr1434=
ENST00000225964.9:c.4302C>T ENSP00000225964.5:p.Thr1434=
NM_000088.3:c.4302C>T , LRG_1t1:c.4302C>T NP_000079.2:p.Thr1434=
XM_005257058.3:c.4032C>T XP_005257115.2:p.Thr1344=
XM_005257059.3:c.3384C>T XP_005257116.2:p.Thr1128=
XM_011524341.1:c.4104C>T XP_011522643.1:p.Thr1368=
XM_005257058.4:c.4032C>T XP_005257115.2:p.Thr1344=
XM_005257059.4:c.3384C>T XP_005257116.2:p.Thr1128=
NM_000088.4:c.4302C>T MANE Select NP_000079.2:p.Thr1434=