Canonical Allele Identifier: CA263149871

Gene: DPF3

Linked Data

• dbSNP Id: rs1026768301
• MyVariant Identifiers: chr14:g.73150565G>T (hg19) ; chr14:g.72683857G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.72683857G>T , CM000676.2:g.72683857G>T	GRCh38
NC_000014.8:g.73150565G>T , CM000676.1:g.73150565G>T	GRCh37
NC_000014.7:g.72220318G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546183.2:n.750+9219C>A
ENST00000556509.6:c.742+9219C>A MANE Select	ENSP00000450518.1:n.742+9219C>A
ENST00000614862.5:c.772+9219C>A	ENSP00000481992.1:n.772+9219C>A
ENST00000366353.8:c.907+9219C>A	ENSP00000381791.3:n.907+9219C>A
ENST00000381216.8:c.742+9219C>A	ENSP00000370614.4:n.742+9219C>A
ENST00000541685.5:c.742+9219C>A	ENSP00000441640.1:n.742+9219C>A
ENST00000546183.1:c.772+9219C>A	ENSP00000444662.1:n.772+9219C>A
ENST00000554594.1:n.220+9219C>A
ENST00000556238.5:n.356+9219C>A
ENST00000556509.5:c.742+9219C>A	ENSP00000450518.1:n.742+9219C>A
ENST00000557704.5:n.454+9219C>A
ENST00000610283.4:c.907+9219C>A	ENSP00000479526.1:n.907+9219C>A
ENST00000614862.4:c.772+9219C>A	ENSP00000481992.1:n.772+9219C>A
NM_001280542.1:c.742+9219C>A	NP_001267471.1:n.742+9219C>A
NM_001280543.1:c.772+9219C>A	NP_001267472.1:n.772+9219C>A
NM_001280544.1:c.907+9219C>A	NP_001267473.1:n.907+9219C>A
NM_012074.4:c.742+9219C>A	NP_036206.3:n.742+9219C>A
XM_011537191.1:c.1000+9219C>A	XP_011535493.1:n.1000+9219C>A
XM_011537192.1:c.1000+9219C>A	XP_011535494.1:n.1000+9219C>A
XM_011537193.1:c.835+9219C>A	XP_011535495.1:n.835+9219C>A
XM_017021670.2:c.742+9219C>A	XP_016877159.1:n.742+9219C>A
XM_017021671.1:c.772+9219C>A	XP_016877160.1:n.772+9219C>A
XM_017021672.1:c.772+9219C>A	XP_016877161.1:n.772+9219C>A
XM_017021673.1:c.712+9219C>A	XP_016877162.1:n.712+9219C>A
NM_012074.5:c.742+9219C>A	NP_036206.3:n.742+9219C>A
NM_001280542.3:c.742+9219C>A MANE Select	NP_001267471.1:n.742+9219C>A
NM_001280543.2:c.772+9219C>A	NP_001267472.1:n.772+9219C>A
NM_001280544.2:c.907+9219C>A	NP_001267473.1:n.907+9219C>A