Canonical Allele Identifier: CA2638709051

Gene: COL1A1

Linked Data

• gnomAD v4: 17-50188451-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50188451A>G , CM000679.2:g.50188451A>G	GRCh38
NC_000017.10:g.48265812A>G , CM000679.1:g.48265812A>G	GRCh37
NC_000017.9:g.45620811A>G	NCBI36
NG_007400.1:g.18189T>C , LRG_1:g.18189T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.3207+79T>C MANE Select	ENSP00000225964.6:n.3207+79T>C
ENST00000225964.9:c.3207+79T>C	ENSP00000225964.5:n.3207+79T>C
ENST00000486572.1:n.104T>C
ENST00000511732.1:n.230T>C
NM_000088.3:c.3207+79T>C , LRG_1t1:c.3207+79T>C	NP_000079.2:n.3207+79T>C
XM_005257058.3:c.2937+79T>C	XP_005257115.2:n.2937+79T>C
XM_005257059.3:c.2289+79T>C	XP_005257116.2:n.2289+79T>C
XM_011524341.1:c.3009+79T>C	XP_011522643.1:n.3009+79T>C
XM_005257058.4:c.2937+79T>C	XP_005257115.2:n.2937+79T>C
XM_005257059.4:c.2289+79T>C	XP_005257116.2:n.2289+79T>C
NM_000088.4:c.3207+79T>C MANE Select	NP_000079.2:n.3207+79T>C