Canonical Allele Identifier: CA2341643103

Gene: ZNF615

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52002027A= , CM000681.2:g.52002027A=	GRCh38
NC_000019.9:g.52505280A= , CM000681.1:g.52505280A=	GRCh37
NC_000019.8:g.57197092A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001199324.2:c.143-119T= MANE Select	NP_001186253.1:n.143-119T=
ENST00000598071.6:c.143-119T= MANE Select	ENSP00000471041.1:n.143-119T=
NM_001199324.1:c.143-119T=	NP_001186253.1:n.143-119T=
NM_001321317.1:c.158-119T=	NP_001308246.1:n.158-119T=
NM_001321317.2:c.158-119T=	NP_001308246.1:n.158-119T=
NM_001321318.1:c.131-119T=	NP_001308247.1:n.131-119T=
NM_001321318.2:c.131-119T=	NP_001308247.1:n.131-119T=
NM_001321319.1:c.143-119T=	NP_001308248.1:n.143-119T=
NM_001321319.2:c.143-119T=	NP_001308248.1:n.143-119T=
NM_001321320.1:c.143-119T=	NP_001308249.1:n.143-119T=
NM_001321320.2:c.143-119T=	NP_001308249.1:n.143-119T=
NM_001321321.1:c.143-119T=	NP_001308250.1:n.143-119T=
NM_001321321.2:c.143-119T=	NP_001308250.1:n.143-119T=
NM_001321322.1:c.143-119T=	NP_001308251.1:n.143-119T=
NM_001321322.2:c.143-119T=	NP_001308251.1:n.143-119T=
NM_001321323.1:c.158-119T=	NP_001308252.1:n.158-119T=
NM_001321323.2:c.158-119T=	NP_001308252.1:n.158-119T=
NM_198480.3:c.143-119T=	NP_940882.3:n.143-119T=
NM_198480.4:c.143-119T=	NP_940882.3:n.143-119T=
ENST00000376716.9:c.143-119T=	ENSP00000365906.4:n.143-119T=
ENST00000391795.7:c.158-119T=	ENSP00000375672.3:n.158-119T=
ENST00000593650.5:c.131-119T=	ENSP00000471202.1:n.131-119T=
ENST00000594083.5:c.143-119T=	ENSP00000471549.1:n.143-119T=
ENST00000597747.5:c.143-119T=	ENSP00000470709.1:n.143-119T=
ENST00000598071.5:c.143-119T=	ENSP00000471041.1:n.143-119T=
ENST00000599115.5:c.158-119T=	ENSP00000470880.1:n.158-119T=
ENST00000599177.5:c.143-119T=	ENSP00000470475.1:n.143-119T=
ENST00000601178.5:c.143-119T=	ENSP00000471608.1:n.143-119T=
ENST00000602063.5:c.143-119T=	ENSP00000473089.1:n.143-119T=
ENST00000618049.4:c.143-119T=	ENSP00000484711.1:n.143-119T=
ENST00000618487.4:c.143-119T=	ENSP00000483676.1:n.143-119T=
XM_011526822.1:c.158-119T=	XP_011525124.1:n.158-119T=
XM_011526823.1:c.143-119T=	XP_011525125.1:n.143-119T=
XM_011526824.1:c.143-119T=	XP_011525126.1:n.143-119T=
XM_011526825.1:c.143-119T=	XP_011525127.1:n.143-119T=
XM_011526826.1:c.143-119T=	XP_011525128.1:n.143-119T=
XM_011526827.1:c.158-119T=	XP_011525129.1:n.158-119T=
XM_011526828.1:c.143-119T=	XP_011525130.1:n.143-119T=
XM_011526829.1:c.-302-119T=	XP_011525131.1:n.-302-119T=
XM_011526829.2:c.-302-119T=	XP_011525131.1:n.-302-119T=
XM_011526830.1:c.-302-119T=	XP_011525132.1:n.-302-119T=
XM_017026648.2:c.143-119T=	XP_016882137.1:n.143-119T=
XM_017026649.2:c.143-119T=	XP_016882138.1:n.143-119T=
XM_017026650.2:c.-302-119T=	XP_016882139.1:n.-302-119T=
XM_017026651.2:c.-302-119T=	XP_016882140.1:n.-302-119T=