Canonical Allele Identifier: CA400192276
Community Standard Title: NM_000088.4(COL1A1):c.4100C>A (p.Thr1367Asn)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185926G>T , CM000679.2:g.50185926G>T GRCh38
NC_000017.10:g.48263287G>T , CM000679.1:g.48263287G>T GRCh37
NC_000017.9:g.45618286G>T NCBI36
NG_007400.1:g.20714C>A , LRG_1:g.20714C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.4100C>A MANE Select NP_000079.2:p.Thr1367Asn
ENST00000225964.10:c.4100C>A MANE Select ENSP00000225964.6:p.Thr1367Asn
NM_000088.3:c.4100C>A , LRG_1t1:c.4100C>A NP_000079.2:p.Thr1367Asn
ENST00000225964.9:c.4100C>A ENSP00000225964.5:p.Thr1367Asn
ENST00000510710.3:n.1065C>A
XM_005257058.3:c.3830C>A XP_005257115.2:p.Thr1277Asn
XM_005257058.4:c.3830C>A XP_005257115.2:p.Thr1277Asn
XM_005257059.3:c.3182C>A XP_005257116.2:p.Thr1061Asn
XM_005257059.4:c.3182C>A XP_005257116.2:p.Thr1061Asn
XM_011524341.1:c.3902C>A XP_011522643.1:p.Thr1301Asn