Canonical Allele Identifier: CA2190278074

Gene: ZFAND6

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80121065A= , CM000677.2:g.80121065A=	GRCh38
NC_000015.9:g.80413407A= , CM000677.1:g.80413407A=	GRCh37
NC_000015.8:g.78200462A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261749.11:c.154+567A= MANE Select	ENSP00000261749.6:n.154+567A=
ENST00000261749.10:c.154+567A=	ENSP00000261749.6:n.154+567A=
ENST00000558087.5:c.154+567A=	ENSP00000453888.1:n.154+567A=
ENST00000558272.5:c.154+567A=	ENSP00000456973.1:n.154+567A=
ENST00000558390.5:c.202+567A=	ENSP00000453308.1:n.202+567A=
ENST00000558494.5:c.154+567A=	ENSP00000454137.1:n.154+567A=
ENST00000558688.5:c.154+567A=	ENSP00000452664.1:n.154+567A=
ENST00000558724.1:c.199+567A=	ENSP00000452625.1:n.199+567A=
ENST00000558997.5:c.154+567A=	ENSP00000453571.1:n.154+567A=
ENST00000559157.5:c.154+567A=	ENSP00000454152.1:n.154+567A=
ENST00000559775.5:c.154+567A=	ENSP00000453709.1:n.154+567A=
ENST00000559835.5:c.154+567A=	ENSP00000453291.1:n.154+567A=
ENST00000560392.5:c.154+567A=	ENSP00000455146.1:n.154+567A=
ENST00000560976.5:c.202+567A=	ENSP00000453710.1:n.202+567A=
ENST00000561060.5:c.154+567A=	ENSP00000452735.1:n.154+567A=
ENST00000564367.5:c.154+567A=	ENSP00000454273.1:n.154+567A=
ENST00000613266.4:c.154+567A=	ENSP00000479071.1:n.154+567A=
ENST00000616533.4:c.154+567A=	ENSP00000478129.1:n.154+567A=
ENST00000618205.4:c.154+567A=	ENSP00000484971.1:n.154+567A=
NM_001242911.1:c.154+567A=	NP_001229840.1:n.154+567A=
NM_001242912.1:c.154+567A=	NP_001229841.1:n.154+567A=
NM_001242913.1:c.154+567A=	NP_001229842.1:n.154+567A=
NM_001242914.1:c.154+567A=	NP_001229843.1:n.154+567A=
NM_001242915.1:c.154+567A=	NP_001229844.1:n.154+567A=
NM_001242916.1:c.154+567A=	NP_001229845.1:n.154+567A=
NM_001242917.1:c.154+567A=	NP_001229846.1:n.154+567A=
NM_001242918.1:c.154+567A=	NP_001229847.1:n.154+567A=
NM_001242919.1:c.154+567A=	NP_001229848.1:n.154+567A=
NM_019006.3:c.154+567A=	NP_061879.2:n.154+567A=
XM_011521683.1:c.196+567A=	XP_011519985.1:n.196+567A=
XM_011521684.1:c.154+567A=	XP_011519986.1:n.154+567A=
XM_011521684.2:c.154+567A=	XP_011519986.1:n.154+567A=
XM_024449955.1:c.154+567A=	XP_024305723.1:n.154+567A=
XM_024449956.1:c.154+567A=	XP_024305724.1:n.154+567A=
XM_024449957.1:c.154+567A=	XP_024305725.1:n.154+567A=
XM_024449958.1:c.154+567A=	XP_024305726.1:n.154+567A=
XM_024449959.1:c.154+567A=	XP_024305727.1:n.154+567A=
XM_024449960.1:c.154+567A=	XP_024305728.1:n.154+567A=
XM_024449961.1:c.154+567A=	XP_024305729.1:n.154+567A=
XM_024449962.1:c.154+567A=	XP_024305730.1:n.154+567A=
XM_024449963.1:c.154+567A=	XP_024305731.1:n.154+567A=
NM_019006.4:c.154+567A= MANE Select	NP_061879.2:n.154+567A=
NM_001242911.2:c.154+567A=	NP_001229840.1:n.154+567A=
NM_001242912.2:c.154+567A=	NP_001229841.1:n.154+567A=
NM_001242913.2:c.154+567A=	NP_001229842.1:n.154+567A=
NM_001242914.2:c.154+567A=	NP_001229843.1:n.154+567A=
NM_001242915.2:c.154+567A=	NP_001229844.1:n.154+567A=
NM_001242916.2:c.154+567A=	NP_001229845.1:n.154+567A=
NM_001242917.2:c.154+567A=	NP_001229846.1:n.154+567A=
NM_001242918.2:c.154+567A=	NP_001229847.1:n.154+567A=