Canonical Allele Identifier: CA2638709064
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188479G>T , CM000679.2:g.50188479G>T GRCh38
NC_000017.10:g.48265840G>T , CM000679.1:g.48265840G>T GRCh37
NC_000017.9:g.45620839G>T NCBI36
NG_007400.1:g.18161C>A , LRG_1:g.18161C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.3207+51C>A MANE Select ENSP00000225964.6:n.3207+51C>A
ENST00000225964.9:c.3207+51C>A ENSP00000225964.5:n.3207+51C>A
ENST00000486572.1:n.76C>A
ENST00000511732.1:n.202C>A
NM_000088.3:c.3207+51C>A , LRG_1t1:c.3207+51C>A NP_000079.2:n.3207+51C>A
XM_005257058.3:c.2937+51C>A XP_005257115.2:n.2937+51C>A
XM_005257059.3:c.2289+51C>A XP_005257116.2:n.2289+51C>A
XM_011524341.1:c.3009+51C>A XP_011522643.1:n.3009+51C>A
XM_005257058.4:c.2937+51C>A XP_005257115.2:n.2937+51C>A
XM_005257059.4:c.2289+51C>A XP_005257116.2:n.2289+51C>A
NM_000088.4:c.3207+51C>A MANE Select NP_000079.2:n.3207+51C>A