Canonical Allele Identifier: CA400200685
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188550T>G , CM000679.2:g.50188550T>G GRCh38
NC_000017.10:g.48265911T>G , CM000679.1:g.48265911T>G GRCh37
NC_000017.9:g.45620910T>G NCBI36
NG_007400.1:g.18090A>C , LRG_1:g.18090A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.3187A>C MANE Select ENSP00000225964.6:p.Ser1063Arg
ENST00000225964.9:c.3187A>C ENSP00000225964.5:p.Ser1063Arg
ENST00000486572.1:n.5A>C
ENST00000511732.1:n.131A>C
NM_000088.3:c.3187A>C , LRG_1t1:c.3187A>C NP_000079.2:p.Ser1063Arg
XM_005257058.3:c.2917A>C XP_005257115.2:p.Ser973Arg
XM_005257059.3:c.2269A>C XP_005257116.2:p.Ser757Arg
XM_011524341.1:c.2989A>C XP_011522643.1:p.Ser997Arg
XM_005257058.4:c.2917A>C XP_005257115.2:p.Ser973Arg
XM_005257059.4:c.2269A>C XP_005257116.2:p.Ser757Arg
NM_000088.4:c.3187A>C MANE Select NP_000079.2:p.Ser1063Arg