Canonical Allele Identifier: CA400190059

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48262902C>G (hg19) ; chr17:g.50185541C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185541C>G , CM000679.2:g.50185541C>G	GRCh38
NC_000017.10:g.48262902C>G , CM000679.1:g.48262902C>G	GRCh37
NC_000017.9:g.45617901C>G	NCBI36
NG_007400.1:g.21099G>C , LRG_1:g.21099G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4356G>C MANE Select	ENSP00000225964.6:p.Gln1452His
ENST00000225964.9:c.4356G>C	ENSP00000225964.5:p.Gln1452His
NM_000088.3:c.4356G>C , LRG_1t1:c.4356G>C	NP_000079.2:p.Gln1452His
XM_005257058.3:c.4086G>C	XP_005257115.2:p.Gln1362His
XM_005257059.3:c.3438G>C	XP_005257116.2:p.Gln1146His
XM_011524341.1:c.4158G>C	XP_011522643.1:p.Gln1386His
XM_005257058.4:c.4086G>C	XP_005257115.2:p.Gln1362His
XM_005257059.4:c.3438G>C	XP_005257116.2:p.Gln1146His
NM_000088.4:c.4356G>C MANE Select	NP_000079.2:p.Gln1452His