Canonical Allele Identifier: CA400190085

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48262904G>T (hg19) ; chr17:g.50185543G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185543G>T , CM000679.2:g.50185543G>T	GRCh38
NC_000017.10:g.48262904G>T , CM000679.1:g.48262904G>T	GRCh37
NC_000017.9:g.45617903G>T	NCBI36
NG_007400.1:g.21097C>A , LRG_1:g.21097C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4354C>A MANE Select	ENSP00000225964.6:p.Gln1452Lys
ENST00000225964.9:c.4354C>A	ENSP00000225964.5:p.Gln1452Lys
NM_000088.3:c.4354C>A , LRG_1t1:c.4354C>A	NP_000079.2:p.Gln1452Lys
XM_005257058.3:c.4084C>A	XP_005257115.2:p.Gln1362Lys
XM_005257059.3:c.3436C>A	XP_005257116.2:p.Gln1146Lys
XM_011524341.1:c.4156C>A	XP_011522643.1:p.Gln1386Lys
XM_005257058.4:c.4084C>A	XP_005257115.2:p.Gln1362Lys
XM_005257059.4:c.3436C>A	XP_005257116.2:p.Gln1146Lys
NM_000088.4:c.4354C>A MANE Select	NP_000079.2:p.Gln1452Lys