Canonical Allele Identifier: CA400191936
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185884G>C , CM000679.2:g.50185884G>C GRCh38
NC_000017.10:g.48263245G>C , CM000679.1:g.48263245G>C GRCh37
NC_000017.9:g.45618244G>C NCBI36
NG_007400.1:g.20756C>G , LRG_1:g.20756C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4142C>G MANE Select ENSP00000225964.6:p.Thr1381Ser
ENST00000225964.9:c.4142C>G ENSP00000225964.5:p.Thr1381Ser
ENST00000510710.3:n.1107C>G
NM_000088.3:c.4142C>G , LRG_1t1:c.4142C>G NP_000079.2:p.Thr1381Ser
XM_005257058.3:c.3872C>G XP_005257115.2:p.Thr1291Ser
XM_005257059.3:c.3224C>G XP_005257116.2:p.Thr1075Ser
XM_011524341.1:c.3944C>G XP_011522643.1:p.Thr1315Ser
XM_005257058.4:c.3872C>G XP_005257115.2:p.Thr1291Ser
XM_005257059.4:c.3224C>G XP_005257116.2:p.Thr1075Ser
NM_000088.4:c.4142C>G MANE Select NP_000079.2:p.Thr1381Ser