Canonical Allele Identifier: CA400192143

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48263272T>G (hg19) ; chr17:g.50185911T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185911T>G , CM000679.2:g.50185911T>G	GRCh38
NC_000017.10:g.48263272T>G , CM000679.1:g.48263272T>G	GRCh37
NC_000017.9:g.45618271T>G	NCBI36
NG_007400.1:g.20729A>C , LRG_1:g.20729A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4115A>C MANE Select	ENSP00000225964.6:p.Asn1372Thr
ENST00000225964.9:c.4115A>C	ENSP00000225964.5:p.Asn1372Thr
ENST00000510710.3:n.1080A>C
NM_000088.3:c.4115A>C , LRG_1t1:c.4115A>C	NP_000079.2:p.Asn1372Thr
XM_005257058.3:c.3845A>C	XP_005257115.2:p.Asn1282Thr
XM_005257059.3:c.3197A>C	XP_005257116.2:p.Asn1066Thr
XM_011524341.1:c.3917A>C	XP_011522643.1:p.Asn1306Thr
XM_005257058.4:c.3845A>C	XP_005257115.2:p.Asn1282Thr
XM_005257059.4:c.3197A>C	XP_005257116.2:p.Asn1066Thr
NM_000088.4:c.4115A>C MANE Select	NP_000079.2:p.Asn1372Thr