Canonical Allele Identifier: CA626689139
Community Standard Title: NM_000088.4(COL1A1):c.334-5C>T
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199458G>A , CM000679.2:g.50199458G>A GRCh38
NC_000017.10:g.48276819G>A , CM000679.1:g.48276819G>A GRCh37
NC_000017.9:g.45631818G>A NCBI36
NG_007400.1:g.7182C>T , LRG_1:g.7182C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.334-5C>T MANE Select NP_000079.2:n.334-5C>T
ENST00000225964.10:c.334-5C>T MANE Select ENSP00000225964.6:n.334-5C>T
NM_000088.3:c.334-5C>T , LRG_1t1:c.334-5C>T NP_000079.2:n.334-5C>T
ENST00000225964.9:c.334-5C>T ENSP00000225964.5:n.334-5C>T
ENST00000474644.1:n.550C>T
ENST00000507689.1:c.388-5C>T ENSP00000460459.1:n.388-5C>T
XM_005257058.3:c.334-5C>T XP_005257115.2:n.334-5C>T
XM_005257058.4:c.334-5C>T XP_005257115.2:n.334-5C>T
XM_005257059.3:c.334-5C>T XP_005257116.2:n.334-5C>T
XM_005257059.4:c.334-5C>T XP_005257116.2:n.334-5C>T
XM_011524341.1:c.334-5C>T XP_011522643.1:n.334-5C>T