Canonical Allele Identifier: CA500991515
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48263145G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185784G>T , CM000679.2:g.50185784G>T GRCh38
NC_000017.10:g.48263145G>T , CM000679.1:g.48263145G>T GRCh37
NC_000017.9:g.45618144G>T NCBI36
NG_007400.1:g.20856C>A , LRG_1:g.20856C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4242C>A MANE Select ENSP00000225964.6:p.Gly1414=
ENST00000225964.9:c.4242C>A ENSP00000225964.5:p.Gly1414=
NM_000088.3:c.4242C>A , LRG_1t1:c.4242C>A NP_000079.2:p.Gly1414=
XM_005257058.3:c.3972C>A XP_005257115.2:p.Gly1324=
XM_005257059.3:c.3324C>A XP_005257116.2:p.Gly1108=
XM_011524341.1:c.4044C>A XP_011522643.1:p.Gly1348=
XM_005257058.4:c.3972C>A XP_005257115.2:p.Gly1324=
XM_005257059.4:c.3324C>A XP_005257116.2:p.Gly1108=
NM_000088.4:c.4242C>A MANE Select NP_000079.2:p.Gly1414=