Canonical Allele Identifier: CA400191838

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48263231T>G (hg19) ; chr17:g.50185870T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185870T>G , CM000679.2:g.50185870T>G	GRCh38
NC_000017.10:g.48263231T>G , CM000679.1:g.48263231T>G	GRCh37
NC_000017.9:g.45618230T>G	NCBI36
NG_007400.1:g.20770A>C , LRG_1:g.20770A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4156A>C MANE Select	ENSP00000225964.6:p.Lys1386Gln
ENST00000225964.9:c.4156A>C	ENSP00000225964.5:p.Lys1386Gln
ENST00000510710.3:n.1121A>C
NM_000088.3:c.4156A>C , LRG_1t1:c.4156A>C	NP_000079.2:p.Lys1386Gln
XM_005257058.3:c.3886A>C	XP_005257115.2:p.Lys1296Gln
XM_005257059.3:c.3238A>C	XP_005257116.2:p.Lys1080Gln
XM_011524341.1:c.3958A>C	XP_011522643.1:p.Lys1320Gln
XM_005257058.4:c.3886A>C	XP_005257115.2:p.Lys1296Gln
XM_005257059.4:c.3238A>C	XP_005257116.2:p.Lys1080Gln
NM_000088.4:c.4156A>C MANE Select	NP_000079.2:p.Lys1386Gln