Canonical Allele Identifier: CA291542789
Community Standard Title: NM_000088.4(COL1A1):c.4237G>A (p.Asp1413Asn)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185789C>T , CM000679.2:g.50185789C>T GRCh38
NC_000017.10:g.48263150C>T , CM000679.1:g.48263150C>T GRCh37
NC_000017.9:g.45618149C>T NCBI36
NG_007400.1:g.20851G>A , LRG_1:g.20851G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.4237G>A MANE Select NP_000079.2:p.Asp1413Asn
ENST00000225964.10:c.4237G>A MANE Select ENSP00000225964.6:p.Asp1413Asn
NM_000088.3:c.4237G>A , LRG_1t1:c.4237G>A NP_000079.2:p.Asp1413Asn
ENST00000225964.9:c.4237G>A ENSP00000225964.5:p.Asp1413Asn
XM_005257058.3:c.3967G>A XP_005257115.2:p.Asp1323Asn
XM_005257058.4:c.3967G>A XP_005257115.2:p.Asp1323Asn
XM_005257059.3:c.3319G>A XP_005257116.2:p.Asp1107Asn
XM_005257059.4:c.3319G>A XP_005257116.2:p.Asp1107Asn
XM_011524341.1:c.4039G>A XP_011522643.1:p.Asp1347Asn