Canonical Allele Identifier: CA10588936

Gene: COL1A1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50186387C>T , CM000679.2:g.50186387C>T	GRCh38
NC_000017.10:g.48263748C>T , CM000679.1:g.48263748C>T	GRCh37
NC_000017.9:g.45618747C>T	NCBI36
NG_007400.1:g.20253G>A , LRG_1:g.20253G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.3935G>A MANE Select	ENSP00000225964.6:p.Trp1312Ter
ENST00000225964.9:c.3935G>A	ENSP00000225964.5:p.Trp1312Ter
ENST00000510710.3:n.604G>A
NM_000088.3:c.3935G>A , LRG_1t1:c.3935G>A	NP_000079.2:p.Trp1312Ter
XM_005257058.3:c.3665G>A	XP_005257115.2:p.Trp1222Ter
XM_005257059.3:c.3017G>A	XP_005257116.2:p.Trp1006Ter
XM_011524341.1:c.3737G>A	XP_011522643.1:p.Trp1246Ter
XM_005257058.4:c.3665G>A	XP_005257115.2:p.Trp1222Ter
XM_005257059.4:c.3017G>A	XP_005257116.2:p.Trp1006Ter
NM_000088.4:c.3935G>A MANE Select	NP_000079.2:p.Trp1312Ter