Canonical Allele Identifier: CA8644392
Community Standard Title: NM_000088.4(COL1A1):c.3580G>A (p.Ala1194Thr)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50186874C>T , CM000679.2:g.50186874C>T GRCh38
NC_000017.10:g.48264235C>T , CM000679.1:g.48264235C>T GRCh37
NC_000017.9:g.45619234C>T NCBI36
NG_007400.1:g.19766G>A , LRG_1:g.19766G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.3580G>A MANE Select NP_000079.2:p.Ala1194Thr
ENST00000225964.10:c.3580G>A MANE Select ENSP00000225964.6:p.Ala1194Thr
NM_000088.3:c.3580G>A , LRG_1t1:c.3580G>A NP_000079.2:p.Ala1194Thr
ENST00000225964.9:c.3580G>A ENSP00000225964.5:p.Ala1194Thr
ENST00000510710.3:n.249G>A
XM_005257058.3:c.3310G>A XP_005257115.2:p.Ala1104Thr
XM_005257058.4:c.3310G>A XP_005257115.2:p.Ala1104Thr
XM_005257059.3:c.2662G>A XP_005257116.2:p.Ala888Thr
XM_005257059.4:c.2662G>A XP_005257116.2:p.Ala888Thr
XM_011524341.1:c.3382G>A XP_011522643.1:p.Ala1128Thr