Canonical Allele Identifier: CA400207934
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50190340A>T , CM000679.2:g.50190340A>T GRCh38
NC_000017.10:g.48267701A>T , CM000679.1:g.48267701A>T GRCh37
NC_000017.9:g.45622700A>T NCBI36
NG_007400.1:g.16300T>A , LRG_1:g.16300T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.2438T>A MANE Select ENSP00000225964.6:p.Phe813Tyr
ENST00000225964.9:c.2438T>A ENSP00000225964.5:p.Phe813Tyr
ENST00000494334.1:n.365T>A
NM_000088.3:c.2438T>A , LRG_1t1:c.2438T>A NP_000079.2:p.Phe813Tyr
XM_005257058.3:c.2438T>A XP_005257115.2:p.Phe813Tyr
XM_005257059.3:c.1520T>A XP_005257116.2:p.Phe507Tyr
XM_011524341.1:c.2240T>A XP_011522643.1:p.Phe747Tyr
XM_005257058.4:c.2438T>A XP_005257115.2:p.Phe813Tyr
XM_005257059.4:c.1520T>A XP_005257116.2:p.Phe507Tyr
NM_000088.4:c.2438T>A MANE Select NP_000079.2:p.Phe813Tyr