Canonical Allele Identifier: CA8645255

Gene: COL1A1

Linked Data

• ClinVar Variation Id: 916235
• ClinVar RCV Id: RCV001171797 ; RCV002393381 ; RCV003517302
• dbSNP Id: rs770169695
• ExAC: 17:48272100 G / A
• gnomAD v2: 17-48272100-G-A
• gnomAD v3: 17-50194739-G-A
• gnomAD v4: 17-50194739-G-A
• MyVariant Identifiers: chr17:g.48272100G>A (hg19) ; chr17:g.50194739G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50194739G>A , CM000679.2:g.50194739G>A	GRCh38
NC_000017.10:g.48272100G>A , CM000679.1:g.48272100G>A	GRCh37
NC_000017.9:g.45627099G>A	NCBI36
NG_007400.1:g.11901C>T , LRG_1:g.11901C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1443C>T MANE Select	ENSP00000225964.6:p.Pro481=
ENST00000225964.9:c.1443C>T	ENSP00000225964.5:p.Pro481=
ENST00000471344.1:n.387C>T
NM_000088.3:c.1443C>T , LRG_1t1:c.1443C>T	NP_000079.2:p.Pro481=
XM_005257058.3:c.1443C>T	XP_005257115.2:p.Pro481=
XM_005257059.3:c.957+1575C>T	XP_005257116.2:n.957+1575C>T
XM_011524341.1:c.1245C>T	XP_011522643.1:p.Pro415=
XM_005257058.4:c.1443C>T	XP_005257115.2:p.Pro481=
XM_005257059.4:c.957+1575C>T	XP_005257116.2:n.957+1575C>T
NM_000088.4:c.1443C>T MANE Select	NP_000079.2:p.Pro481=