Canonical Allele Identifier: CA500845770
Community Standard Title: NM_000088.4(COL1A1):c.2400A>G (p.Gly800=)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50190378T>C , CM000679.2:g.50190378T>C GRCh38
NC_000017.10:g.48267739T>C , CM000679.1:g.48267739T>C GRCh37
NC_000017.9:g.45622738T>C NCBI36
NG_007400.1:g.16262A>G , LRG_1:g.16262A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.2400A>G MANE Select NP_000079.2:p.Gly800=
ENST00000225964.10:c.2400A>G MANE Select ENSP00000225964.6:p.Gly800=
NM_000088.3:c.2400A>G , LRG_1t1:c.2400A>G NP_000079.2:p.Gly800=
ENST00000225964.9:c.2400A>G ENSP00000225964.5:p.Gly800=
ENST00000494334.1:n.327A>G
XM_005257058.3:c.2400A>G XP_005257115.2:p.Gly800=
XM_005257058.4:c.2400A>G XP_005257115.2:p.Gly800=
XM_005257059.3:c.1482A>G XP_005257116.2:p.Gly494=
XM_005257059.4:c.1482A>G XP_005257116.2:p.Gly494=
XM_011524341.1:c.2202A>G XP_011522643.1:p.Gly734=