Canonical Allele Identifier: CA8644219
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185778C>T , CM000679.2:g.50185778C>T GRCh38
NC_000017.10:g.48263139C>T , CM000679.1:g.48263139C>T GRCh37
NC_000017.9:g.45618138C>T NCBI36
NG_007400.1:g.20862G>A , LRG_1:g.20862G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.4248G>A MANE Select NP_000079.2:p.Thr1416=
ENST00000225964.10:c.4248G>A MANE Select ENSP00000225964.6:p.Thr1416=
NM_000088.3:c.4248G>A , LRG_1t1:c.4248G>A NP_000079.2:p.Thr1416=
ENST00000225964.9:c.4248G>A ENSP00000225964.5:p.Thr1416=
XM_005257058.3:c.3978G>A XP_005257115.2:p.Thr1326=
XM_005257058.4:c.3978G>A XP_005257115.2:p.Thr1326=
XM_005257059.3:c.3330G>A XP_005257116.2:p.Thr1110=
XM_005257059.4:c.3330G>A XP_005257116.2:p.Thr1110=
XM_011524341.1:c.4050G>A XP_011522643.1:p.Thr1350=