Canonical Allele Identifier: CA1350486740

Gene: ZNF385D

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.21664877G= , CM000665.2:g.21664877G=	GRCh38
NC_000003.11:g.21706369G= , CM000665.1:g.21706369G=	GRCh37
NC_000003.10:g.21681373G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446749.2:c.165+9C=	ENSP00000388232.1:n.165+9C=
ENST00000494108.3:c.468+9C=	ENSP00000495609.3:n.468+9C=
ENST00000706131.1:c.468+9C=	ENSP00000516216.1:n.468+9C=
ENST00000706132.1:c.165+9C=	ENSP00000516217.1:n.165+9C=
ENST00000706133.1:c.*64+9C=	ENSP00000516218.1:n.*64+9C=
ENST00000706134.1:c.156+9C=	ENSP00000516219.1:n.156+9C=
ENST00000706135.1:c.*64+9C=	ENSP00000516220.1:n.*64+9C=
ENST00000706136.1:c.530+9C=	ENSP00000516221.1:n.530+9C=
ENST00000706137.1:c.*271+9C=	ENSP00000516222.1:n.*271+9C=
ENST00000706138.1:c.*278+9C=	ENSP00000516223.1:n.*278+9C=
ENST00000281523.8:c.165+9C= MANE Select	ENSP00000281523.2:n.165+9C=
ENST00000494108.2:c.468+9C=	ENSP00000495609.2:n.468+9C=
ENST00000281523.7:c.165+9C=	ENSP00000281523.2:n.165+9C=
ENST00000446749.1:c.165+9C=	ENSP00000388232.1:n.165+9C=
ENST00000478967.5:n.312+9C=
ENST00000494108.1:n.889+9C=
ENST00000494118.5:n.467-100193C=
NM_024697.2:c.165+9C=	NP_078973.1:n.165+9C=
XM_005265485.2:c.468+9C=	XP_005265542.1:n.468+9C=
XM_005265486.2:c.468+9C=	XP_005265543.1:n.468+9C=
XM_005265487.2:c.165+9C=	XP_005265544.1:n.165+9C=
XM_011534114.1:c.318+9C=	XP_011532416.1:n.318+9C=
XM_011534115.1:c.255+9C=	XP_011532417.1:n.255+9C=
XM_011534116.1:c.216+9C=	XP_011532418.1:n.216+9C=
XM_011534117.1:c.210+9C=	XP_011532419.1:n.210+9C=
XM_011534118.1:c.165+9C=	XP_011532420.1:n.165+9C=
XM_011534119.1:c.10-100193C=	XP_011532421.1:n.10-100193C=
XM_011534121.1:c.468+9C=	XP_011532423.1:n.468+9C=
XM_011534122.1:c.468+9C=	XP_011532424.1:n.468+9C=
XM_011534123.1:c.468+9C=	XP_011532425.1:n.468+9C=
XM_011534124.1:c.468+9C=	XP_011532426.1:n.468+9C=
XM_011534126.1:c.468+9C=	XP_011532428.1:n.468+9C=
XM_011534127.1:c.468+9C=	XP_011532429.1:n.468+9C=
XM_011534128.1:c.468+9C=	XP_011532430.1:n.468+9C=
XM_011534129.1:c.468+9C=	XP_011532431.1:n.468+9C=
XM_011534122.2:c.468+9C=	XP_011532424.1:n.468+9C=
XM_011534123.2:c.468+9C=	XP_011532425.1:n.468+9C=
XM_011534124.3:c.468+9C=	XP_011532426.1:n.468+9C=
XM_017007191.1:c.468+9C=	XP_016862680.1:n.468+9C=
XM_017007192.1:c.468+9C=	XP_016862681.1:n.468+9C=
XM_017007193.1:c.255+9C=	XP_016862682.1:n.255+9C=
XM_017007194.1:c.216+9C=	XP_016862683.1:n.216+9C=
XM_017007195.1:c.210+9C=	XP_016862684.1:n.210+9C=
XM_017007196.1:c.165+9C=	XP_016862685.1:n.165+9C=
XM_017007197.1:c.156+9C=	XP_016862686.1:n.156+9C=
XM_017007198.1:c.153+9C=	XP_016862687.1:n.153+9C=
XM_017007199.1:c.10-100193C=	XP_016862688.1:n.10-100193C=
XM_017007203.1:c.468+9C=	XP_016862692.1:n.468+9C=
XM_024453754.1:c.210+9C=	XP_024309522.1:n.210+9C=
NM_024697.3:c.165+9C= MANE Select	NP_078973.1:n.165+9C=