Canonical Allele Identifier: CA400190742
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185627T>A , CM000679.2:g.50185627T>A GRCh38
NC_000017.10:g.48262988T>A , CM000679.1:g.48262988T>A GRCh37
NC_000017.9:g.45617987T>A NCBI36
NG_007400.1:g.21013A>T , LRG_1:g.21013A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4270A>T MANE Select ENSP00000225964.6:p.Lys1424Ter
ENST00000225964.9:c.4270A>T ENSP00000225964.5:p.Lys1424Ter
NM_000088.3:c.4270A>T , LRG_1t1:c.4270A>T NP_000079.2:p.Lys1424Ter
XM_005257058.3:c.4000A>T XP_005257115.2:p.Lys1334Ter
XM_005257059.3:c.3352A>T XP_005257116.2:p.Lys1118Ter
XM_011524341.1:c.4072A>T XP_011522643.1:p.Lys1358Ter
XM_005257058.4:c.4000A>T XP_005257115.2:p.Lys1334Ter
XM_005257059.4:c.3352A>T XP_005257116.2:p.Lys1118Ter
NM_000088.4:c.4270A>T MANE Select NP_000079.2:p.Lys1424Ter