Canonical Allele Identifier: CA8645428
Community Standard Title: NM_000088.4(COL1A1):c.1018G>A (p.Ala340Thr)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195961C>T , CM000679.2:g.50195961C>T GRCh38
NC_000017.10:g.48273322C>T , CM000679.1:g.48273322C>T GRCh37
NC_000017.9:g.45628321C>T NCBI36
NG_007400.1:g.10679G>A , LRG_1:g.10679G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.1018G>A MANE Select NP_000079.2:p.Ala340Thr
ENST00000225964.10:c.1018G>A MANE Select ENSP00000225964.6:p.Ala340Thr
NM_000088.3:c.1018G>A , LRG_1t1:c.1018G>A NP_000079.2:p.Ala340Thr
ENST00000225964.9:c.1018G>A ENSP00000225964.5:p.Ala340Thr
XM_005257058.3:c.1018G>A XP_005257115.2:p.Ala340Thr
XM_005257058.4:c.1018G>A XP_005257115.2:p.Ala340Thr
XM_005257059.3:c.957+353G>A XP_005257116.2:n.957+353G>A
XM_005257059.4:c.957+353G>A XP_005257116.2:n.957+353G>A
XM_011524341.1:c.957+353G>A XP_011522643.1:n.957+353G>A