Canonical Allele Identifier: CA2638676142
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195919T>A , CM000679.2:g.50195919T>A GRCh38
NC_000017.10:g.48273280T>A , CM000679.1:g.48273280T>A GRCh37
NC_000017.9:g.45628279T>A NCBI36
NG_007400.1:g.10721A>T , LRG_1:g.10721A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1056+4A>T MANE Select ENSP00000225964.6:n.1056+4A>T
ENST00000225964.9:c.1056+4A>T ENSP00000225964.5:n.1056+4A>T
NM_000088.3:c.1056+4A>T , LRG_1t1:c.1056+4A>T NP_000079.2:n.1056+4A>T
XM_005257058.3:c.1056+4A>T XP_005257115.2:n.1056+4A>T
XM_005257059.3:c.957+395A>T XP_005257116.2:n.957+395A>T
XM_011524341.1:c.957+395A>T XP_011522643.1:n.957+395A>T
XM_005257058.4:c.1056+4A>T XP_005257115.2:n.1056+4A>T
XM_005257059.4:c.957+395A>T XP_005257116.2:n.957+395A>T
NM_000088.4:c.1056+4A>T MANE Select NP_000079.2:n.1056+4A>T