Canonical Allele Identifier: CA400228606
Community Standard Title: NM_000088.4(COL1A1):c.141C>A (p.Tyr47Ter)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199910G>T , CM000679.2:g.50199910G>T GRCh38
NC_000017.10:g.48277271G>T , CM000679.1:g.48277271G>T GRCh37
NC_000017.9:g.45632270G>T NCBI36
NG_007400.1:g.6730C>A , LRG_1:g.6730C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.141C>A MANE Select NP_000079.2:p.Tyr47Ter
ENST00000225964.10:c.141C>A MANE Select ENSP00000225964.6:p.Tyr47Ter
NM_000088.3:c.141C>A , LRG_1t1:c.141C>A NP_000079.2:p.Tyr47Ter
ENST00000225964.9:c.141C>A ENSP00000225964.5:p.Tyr47Ter
ENST00000474644.1:n.260C>A
ENST00000507689.1:c.195C>A ENSP00000460459.1:p.Tyr65Ter
XM_005257058.3:c.141C>A XP_005257115.2:p.Tyr47Ter
XM_005257058.4:c.141C>A XP_005257115.2:p.Tyr47Ter
XM_005257059.3:c.141C>A XP_005257116.2:p.Tyr47Ter
XM_005257059.4:c.141C>A XP_005257116.2:p.Tyr47Ter
XM_011524341.1:c.141C>A XP_011522643.1:p.Tyr47Ter