Canonical Allele Identifier: CA141214839

Gene: COL19A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.70031317A>G , CM000668.2:g.70031317A>G	GRCh38
NC_000006.11:g.70741209A>G , CM000668.1:g.70741209A>G	GRCh37
NC_000006.10:g.70797930A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001858.6:c.1081-2928A>G MANE Select	NP_001849.2:n.1081-2928A>G
ENST00000620364.5:c.1081-2928A>G MANE Select	ENSP00000480474.1:n.1081-2928A>G
NM_001858.5:c.1081-2928A>G	NP_001849.2:n.1081-2928A>G
ENST00000620364.4:c.1081-2928A>G	ENSP00000480474.1:n.1081-2928A>G
XM_011535437.1:c.1156-2928A>G	XP_011533739.1:n.1156-2928A>G
XM_011535437.2:c.1156-2928A>G	XP_011533739.1:n.1156-2928A>G
XM_011535438.1:c.1081-2928A>G	XP_011533740.1:n.1081-2928A>G
XM_011535438.2:c.1081-2928A>G	XP_011533740.1:n.1081-2928A>G
XM_017010253.1:c.1156-2928A>G	XP_016865742.1:n.1156-2928A>G
XM_017010254.1:c.1102-2928A>G	XP_016865743.1:n.1102-2928A>G
XM_017010255.1:c.1081-2928A>G	XP_016865744.1:n.1081-2928A>G
XM_017010256.1:c.1081-2928A>G	XP_016865745.1:n.1081-2928A>G
XM_017010257.1:c.1030-2928A>G	XP_016865746.1:n.1030-2928A>G
XM_017010258.1:c.955-2928A>G	XP_016865747.1:n.955-2928A>G
XM_017010259.1:c.1156-2928A>G	XP_016865748.1:n.1156-2928A>G