Canonical Allele Identifier: CA400191764

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48263214C>G (hg19) ; chr17:g.50185853C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185853C>G , CM000679.2:g.50185853C>G	GRCh38
NC_000017.10:g.48263214C>G , CM000679.1:g.48263214C>G	GRCh37
NC_000017.9:g.45618213C>G	NCBI36
NG_007400.1:g.20787G>C , LRG_1:g.20787G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4173G>C MANE Select	ENSP00000225964.6:p.Gln1391His
ENST00000225964.9:c.4173G>C	ENSP00000225964.5:p.Gln1391His
ENST00000510710.3:n.1138G>C
NM_000088.3:c.4173G>C , LRG_1t1:c.4173G>C	NP_000079.2:p.Gln1391His
XM_005257058.3:c.3903G>C	XP_005257115.2:p.Gln1301His
XM_005257059.3:c.3255G>C	XP_005257116.2:p.Gln1085His
XM_011524341.1:c.3975G>C	XP_011522643.1:p.Gln1325His
XM_005257058.4:c.3903G>C	XP_005257115.2:p.Gln1301His
XM_005257059.4:c.3255G>C	XP_005257116.2:p.Gln1085His
NM_000088.4:c.4173G>C MANE Select	NP_000079.2:p.Gln1391His