Canonical Allele Identifier: CA400201506

Gene: COL1A1

Linked Data

• dbSNP Id: rs1906772457
• MyVariant Identifiers: chr17:g.48265994T>G (hg19) ; chr17:g.50188633T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50188633T>G , CM000679.2:g.50188633T>G	GRCh38
NC_000017.10:g.48265994T>G , CM000679.1:g.48265994T>G	GRCh37
NC_000017.9:g.45620993T>G	NCBI36
NG_007400.1:g.18007A>C , LRG_1:g.18007A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.3104A>C MANE Select	ENSP00000225964.6:p.Asp1035Ala
ENST00000225964.9:c.3104A>C	ENSP00000225964.5:p.Asp1035Ala
ENST00000511732.1:n.48A>C
NM_000088.3:c.3104A>C , LRG_1t1:c.3104A>C	NP_000079.2:p.Asp1035Ala
XM_005257058.3:c.2834A>C	XP_005257115.2:p.Asp945Ala
XM_005257059.3:c.2186A>C	XP_005257116.2:p.Asp729Ala
XM_011524341.1:c.2906A>C	XP_011522643.1:p.Asp969Ala
XM_005257058.4:c.2834A>C	XP_005257115.2:p.Asp945Ala
XM_005257059.4:c.2186A>C	XP_005257116.2:p.Asp729Ala
NM_000088.4:c.3104A>C MANE Select	NP_000079.2:p.Asp1035Ala