Canonical Allele Identifier: CA291542796

Gene: COL1A1

Linked Data

• dbSNP Id: rs1028377152
• gnomAD v2: 17-48263237-G-A
• gnomAD v3: 17-50185876-G-A
• gnomAD v4: 17-50185876-G-A
• MyVariant Identifiers: chr17:g.48263237G>A (hg19) ; chr17:g.50185876G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185876G>A , CM000679.2:g.50185876G>A	GRCh38
NC_000017.10:g.48263237G>A , CM000679.1:g.48263237G>A	GRCh37
NC_000017.9:g.45618236G>A	NCBI36
NG_007400.1:g.20764C>T , LRG_1:g.20764C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4150C>T MANE Select	ENSP00000225964.6:p.Leu1384Phe
ENST00000225964.9:c.4150C>T	ENSP00000225964.5:p.Leu1384Phe
ENST00000510710.3:n.1115C>T
NM_000088.3:c.4150C>T , LRG_1t1:c.4150C>T	NP_000079.2:p.Leu1384Phe
XM_005257058.3:c.3880C>T	XP_005257115.2:p.Leu1294Phe
XM_005257059.3:c.3232C>T	XP_005257116.2:p.Leu1078Phe
XM_011524341.1:c.3952C>T	XP_011522643.1:p.Leu1318Phe
XM_005257058.4:c.3880C>T	XP_005257115.2:p.Leu1294Phe
XM_005257059.4:c.3232C>T	XP_005257116.2:p.Leu1078Phe
NM_000088.4:c.4150C>T MANE Select	NP_000079.2:p.Leu1384Phe