Canonical Allele Identifier: CA400227952
Community Standard Title: NM_000088.4(COL1A1):c.299-1G>C
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199591C>G , CM000679.2:g.50199591C>G GRCh38
NC_000017.10:g.48276952C>G , CM000679.1:g.48276952C>G GRCh37
NC_000017.9:g.45631951C>G NCBI36
NG_007400.1:g.7049G>C , LRG_1:g.7049G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.299-1G>C MANE Select NP_000079.2:n.299-1G>C
ENST00000225964.10:c.299-1G>C MANE Select ENSP00000225964.6:n.299-1G>C
NM_000088.3:c.299-1G>C , LRG_1t1:c.299-1G>C NP_000079.2:n.299-1G>C
ENST00000225964.9:c.299-1G>C ENSP00000225964.5:n.299-1G>C
ENST00000474644.1:n.418-1G>C
ENST00000507689.1:c.353-1G>C ENSP00000460459.1:n.353-1G>C
XM_005257058.3:c.299-1G>C XP_005257115.2:n.299-1G>C
XM_005257058.4:c.299-1G>C XP_005257115.2:n.299-1G>C
XM_005257059.3:c.299-1G>C XP_005257116.2:n.299-1G>C
XM_005257059.4:c.299-1G>C XP_005257116.2:n.299-1G>C
XM_011524341.1:c.299-1G>C XP_011522643.1:n.299-1G>C