Canonical Allele Identifier: CA400221400
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196186T>A , CM000679.2:g.50196186T>A GRCh38
NC_000017.10:g.48273547T>A , CM000679.1:g.48273547T>A GRCh37
NC_000017.9:g.45628546T>A NCBI36
NG_007400.1:g.10454A>T , LRG_1:g.10454A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.971A>T MANE Select ENSP00000225964.6:p.Asn324Ile
ENST00000225964.9:c.971A>T ENSP00000225964.5:p.Asn324Ile
ENST00000485870.1:n.296A>T
NM_000088.3:c.971A>T , LRG_1t1:c.971A>T NP_000079.2:p.Asn324Ile
XM_005257058.3:c.971A>T XP_005257115.2:p.Asn324Ile
XM_005257059.3:c.957+128A>T XP_005257116.2:n.957+128A>T
XM_011524341.1:c.957+128A>T XP_011522643.1:n.957+128A>T
XM_005257058.4:c.971A>T XP_005257115.2:p.Asn324Ile
XM_005257059.4:c.957+128A>T XP_005257116.2:n.957+128A>T
NM_000088.4:c.971A>T MANE Select NP_000079.2:p.Asn324Ile