Canonical Allele Identifier: CA2638676883
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196293C>T , CM000679.2:g.50196293C>T GRCh38
NC_000017.10:g.48273654C>T , CM000679.1:g.48273654C>T GRCh37
NC_000017.9:g.45628653C>T NCBI36
NG_007400.1:g.10347G>A , LRG_1:g.10347G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.957+21G>A MANE Select ENSP00000225964.6:n.957+21G>A
ENST00000225964.9:c.957+21G>A ENSP00000225964.5:n.957+21G>A
ENST00000485870.1:n.282+21G>A
NM_000088.3:c.957+21G>A , LRG_1t1:c.957+21G>A NP_000079.2:n.957+21G>A
XM_005257058.3:c.957+21G>A XP_005257115.2:n.957+21G>A
XM_005257059.3:c.957+21G>A XP_005257116.2:n.957+21G>A
XM_011524341.1:c.957+21G>A XP_011522643.1:n.957+21G>A
XM_005257058.4:c.957+21G>A XP_005257115.2:n.957+21G>A
XM_005257059.4:c.957+21G>A XP_005257116.2:n.957+21G>A
NM_000088.4:c.957+21G>A MANE Select NP_000079.2:n.957+21G>A