Canonical Allele Identifier: CA400200523

Gene: COL1A1

Linked Data

• dbSNP Id: rs766795631
• MyVariant Identifiers: chr17:g.48265893T>C (hg19) ; chr17:g.50188532T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50188532T>C , CM000679.2:g.50188532T>C	GRCh38
NC_000017.10:g.48265893T>C , CM000679.1:g.48265893T>C	GRCh37
NC_000017.9:g.45620892T>C	NCBI36
NG_007400.1:g.18108A>G , LRG_1:g.18108A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.3205A>G MANE Select	ENSP00000225964.6:p.Thr1069Ala
ENST00000225964.9:c.3205A>G	ENSP00000225964.5:p.Thr1069Ala
ENST00000486572.1:n.23A>G
ENST00000511732.1:n.149A>G
NM_000088.3:c.3205A>G , LRG_1t1:c.3205A>G	NP_000079.2:p.Thr1069Ala
XM_005257058.3:c.2935A>G	XP_005257115.2:p.Thr979Ala
XM_005257059.3:c.2287A>G	XP_005257116.2:p.Thr763Ala
XM_011524341.1:c.3007A>G	XP_011522643.1:p.Thr1003Ala
XM_005257058.4:c.2935A>G	XP_005257115.2:p.Thr979Ala
XM_005257059.4:c.2287A>G	XP_005257116.2:p.Thr763Ala
NM_000088.4:c.3205A>G MANE Select	NP_000079.2:p.Thr1069Ala