Canonical Allele Identifier: CA8644553

Gene: COL1A1

Linked Data

• dbSNP Id: rs558106162
• ExAC: 17:48265968 G / A
• gnomAD v2: 17-48265968-G-A
• gnomAD v3: 17-50188607-G-A
• gnomAD v4: 17-50188607-G-A
• MyVariant Identifiers: chr17:g.48265968G>A (hg19) ; chr17:g.50188607G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50188607G>A , CM000679.2:g.50188607G>A	GRCh38
NC_000017.10:g.48265968G>A , CM000679.1:g.48265968G>A	GRCh37
NC_000017.9:g.45620967G>A	NCBI36
NG_007400.1:g.18033C>T , LRG_1:g.18033C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.3130C>T MANE Select	ENSP00000225964.6:p.Pro1044Ser
ENST00000225964.9:c.3130C>T	ENSP00000225964.5:p.Pro1044Ser
ENST00000511732.1:n.74C>T
NM_000088.3:c.3130C>T , LRG_1t1:c.3130C>T	NP_000079.2:p.Pro1044Ser
XM_005257058.3:c.2860C>T	XP_005257115.2:p.Pro954Ser
XM_005257059.3:c.2212C>T	XP_005257116.2:p.Pro738Ser
XM_011524341.1:c.2932C>T	XP_011522643.1:p.Pro978Ser
XM_005257058.4:c.2860C>T	XP_005257115.2:p.Pro954Ser
XM_005257059.4:c.2212C>T	XP_005257116.2:p.Pro738Ser
NM_000088.4:c.3130C>T MANE Select	NP_000079.2:p.Pro1044Ser