Canonical Allele Identifier: CA400227442
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199296A>C , CM000679.2:g.50199296A>C GRCh38
NC_000017.10:g.48276657A>C , CM000679.1:g.48276657A>C GRCh37
NC_000017.9:g.45631656A>C NCBI36
NG_007400.1:g.7344T>G , LRG_1:g.7344T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.401T>G MANE Select ENSP00000225964.6:p.Ile134Ser
ENST00000225964.9:c.401T>G ENSP00000225964.5:p.Ile134Ser
ENST00000474644.1:n.622T>G
ENST00000507689.1:c.455T>G ENSP00000460459.1:p.Ile152Ser
NM_000088.3:c.401T>G , LRG_1t1:c.401T>G NP_000079.2:p.Ile134Ser
XM_005257058.3:c.401T>G XP_005257115.2:p.Ile134Ser
XM_005257059.3:c.401T>G XP_005257116.2:p.Ile134Ser
XM_011524341.1:c.401T>G XP_011522643.1:p.Ile134Ser
XM_005257058.4:c.401T>G XP_005257115.2:p.Ile134Ser
XM_005257059.4:c.401T>G XP_005257116.2:p.Ile134Ser
NM_000088.4:c.401T>G MANE Select NP_000079.2:p.Ile134Ser