Canonical Allele Identifier: CA8645457
Community Standard Title: NM_000088.4(COL1A1):c.979G>T (p.Ala327Ser)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196178C>A , CM000679.2:g.50196178C>A GRCh38
NC_000017.10:g.48273539C>A , CM000679.1:g.48273539C>A GRCh37
NC_000017.9:g.45628538C>A NCBI36
NG_007400.1:g.10462G>T , LRG_1:g.10462G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.979G>T MANE Select NP_000079.2:p.Ala327Ser
ENST00000225964.10:c.979G>T MANE Select ENSP00000225964.6:p.Ala327Ser
NM_000088.3:c.979G>T , LRG_1t1:c.979G>T NP_000079.2:p.Ala327Ser
ENST00000225964.9:c.979G>T ENSP00000225964.5:p.Ala327Ser
ENST00000485870.1:n.304G>T
XM_005257058.3:c.979G>T XP_005257115.2:p.Ala327Ser
XM_005257058.4:c.979G>T XP_005257115.2:p.Ala327Ser
XM_005257059.3:c.957+136G>T XP_005257116.2:n.957+136G>T
XM_005257059.4:c.957+136G>T XP_005257116.2:n.957+136G>T
XM_011524341.1:c.957+136G>T XP_011522643.1:n.957+136G>T