Canonical Allele Identifier: CA8645057
Community Standard Title: NM_000088.4(COL1A1):c.1861C>A (p.Pro621Thr)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192811G>T , CM000679.2:g.50192811G>T GRCh38
NC_000017.10:g.48270172G>T , CM000679.1:g.48270172G>T GRCh37
NC_000017.9:g.45625171G>T NCBI36
NG_007400.1:g.13829C>A , LRG_1:g.13829C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.1861C>A MANE Select NP_000079.2:p.Pro621Thr
ENST00000225964.10:c.1861C>A MANE Select ENSP00000225964.6:p.Pro621Thr
NM_000088.3:c.1861C>A , LRG_1t1:c.1861C>A NP_000079.2:p.Pro621Thr
ENST00000225964.9:c.1861C>A ENSP00000225964.5:p.Pro621Thr
ENST00000476387.1:n.210C>A
XM_005257058.3:c.1861C>A XP_005257115.2:p.Pro621Thr
XM_005257058.4:c.1861C>A XP_005257115.2:p.Pro621Thr
XM_005257059.3:c.958-118C>A XP_005257116.2:n.958-118C>A
XM_005257059.4:c.958-118C>A XP_005257116.2:n.958-118C>A
XM_011524341.1:c.1663C>A XP_011522643.1:p.Pro555Thr