Canonical Allele Identifier: CA400197195
Community Standard Title: NM_000088.4(COL1A1):c.3677A>G (p.Asp1226Gly)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50186777T>C , CM000679.2:g.50186777T>C GRCh38
NC_000017.10:g.48264138T>C , CM000679.1:g.48264138T>C GRCh37
NC_000017.9:g.45619137T>C NCBI36
NG_007400.1:g.19863A>G , LRG_1:g.19863A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.3677A>G MANE Select NP_000079.2:p.Asp1226Gly
ENST00000225964.10:c.3677A>G MANE Select ENSP00000225964.6:p.Asp1226Gly
NM_000088.3:c.3677A>G , LRG_1t1:c.3677A>G NP_000079.2:p.Asp1226Gly
ENST00000225964.9:c.3677A>G ENSP00000225964.5:p.Asp1226Gly
ENST00000510710.3:n.346A>G
XM_005257058.3:c.3407A>G XP_005257115.2:p.Asp1136Gly
XM_005257058.4:c.3407A>G XP_005257115.2:p.Asp1136Gly
XM_005257059.3:c.2759A>G XP_005257116.2:p.Asp920Gly
XM_005257059.4:c.2759A>G XP_005257116.2:p.Asp920Gly
XM_011524341.1:c.3479A>G XP_011522643.1:p.Asp1160Gly