Canonical Allele Identifier: CA8644223
Community Standard Title: NM_000088.4(COL1A1):c.4228G>A (p.Val1410Ile)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185798C>T , CM000679.2:g.50185798C>T GRCh38
NC_000017.10:g.48263159C>T , CM000679.1:g.48263159C>T GRCh37
NC_000017.9:g.45618158C>T NCBI36
NG_007400.1:g.20842G>A , LRG_1:g.20842G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.4228G>A MANE Select NP_000079.2:p.Val1410Ile
ENST00000225964.10:c.4228G>A MANE Select ENSP00000225964.6:p.Val1410Ile
NM_000088.3:c.4228G>A , LRG_1t1:c.4228G>A NP_000079.2:p.Val1410Ile
ENST00000225964.9:c.4228G>A ENSP00000225964.5:p.Val1410Ile
XM_005257058.3:c.3958G>A XP_005257115.2:p.Val1320Ile
XM_005257058.4:c.3958G>A XP_005257115.2:p.Val1320Ile
XM_005257059.3:c.3310G>A XP_005257116.2:p.Val1104Ile
XM_005257059.4:c.3310G>A XP_005257116.2:p.Val1104Ile
XM_011524341.1:c.4030G>A XP_011522643.1:p.Val1344Ile