Canonical Allele Identifier: CA400192047

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48263261A>C (hg19) ; chr17:g.50185900A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185900A>C , CM000679.2:g.50185900A>C	GRCh38
NC_000017.10:g.48263261A>C , CM000679.1:g.48263261A>C	GRCh37
NC_000017.9:g.45618260A>C	NCBI36
NG_007400.1:g.20740T>G , LRG_1:g.20740T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4126T>G MANE Select	ENSP00000225964.6:p.Tyr1376Asp
ENST00000225964.9:c.4126T>G	ENSP00000225964.5:p.Tyr1376Asp
ENST00000510710.3:n.1091T>G
NM_000088.3:c.4126T>G , LRG_1t1:c.4126T>G	NP_000079.2:p.Tyr1376Asp
XM_005257058.3:c.3856T>G	XP_005257115.2:p.Tyr1286Asp
XM_005257059.3:c.3208T>G	XP_005257116.2:p.Tyr1070Asp
XM_011524341.1:c.3928T>G	XP_011522643.1:p.Tyr1310Asp
XM_005257058.4:c.3856T>G	XP_005257115.2:p.Tyr1286Asp
XM_005257059.4:c.3208T>G	XP_005257116.2:p.Tyr1070Asp
NM_000088.4:c.4126T>G MANE Select	NP_000079.2:p.Tyr1376Asp