Canonical Allele Identifier: CA400205049
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50189239C>G , CM000679.2:g.50189239C>G GRCh38
NC_000017.10:g.48266600C>G , CM000679.1:g.48266600C>G GRCh37
NC_000017.9:g.45621599C>G NCBI36
NG_007400.1:g.17401G>C , LRG_1:g.17401G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.2866G>C MANE Select ENSP00000225964.6:p.Gly956Arg
ENST00000225964.9:c.2866G>C ENSP00000225964.5:p.Gly956Arg
NM_000088.3:c.2866G>C , LRG_1t1:c.2866G>C NP_000079.2:p.Gly956Arg
XM_005257058.3:c.2668-229G>C XP_005257115.2:n.2668-229G>C
XM_005257059.3:c.1948G>C XP_005257116.2:p.Gly650Arg
XM_011524341.1:c.2668G>C XP_011522643.1:p.Gly890Arg
XM_005257058.4:c.2668-229G>C XP_005257115.2:n.2668-229G>C
XM_005257059.4:c.1948G>C XP_005257116.2:p.Gly650Arg
NM_000088.4:c.2866G>C MANE Select NP_000079.2:p.Gly956Arg