Canonical Allele Identifier: CA400218439
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194806G>C , CM000679.2:g.50194806G>C GRCh38
NC_000017.10:g.48272167G>C , CM000679.1:g.48272167G>C GRCh37
NC_000017.9:g.45627166G>C NCBI36
NG_007400.1:g.11834C>G , LRG_1:g.11834C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1376C>G MANE Select ENSP00000225964.6:p.Pro459Arg
ENST00000225964.9:c.1376C>G ENSP00000225964.5:p.Pro459Arg
ENST00000471344.1:n.320C>G
NM_000088.3:c.1376C>G , LRG_1t1:c.1376C>G NP_000079.2:p.Pro459Arg
XM_005257058.3:c.1376C>G XP_005257115.2:p.Pro459Arg
XM_005257059.3:c.957+1508C>G XP_005257116.2:n.957+1508C>G
XM_011524341.1:c.1178C>G XP_011522643.1:p.Pro393Arg
XM_005257058.4:c.1376C>G XP_005257115.2:p.Pro459Arg
XM_005257059.4:c.957+1508C>G XP_005257116.2:n.957+1508C>G
NM_000088.4:c.1376C>G MANE Select NP_000079.2:p.Pro459Arg