Canonical Allele Identifier: CA1884217403

Gene: SNAPC4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136390000A= , CM000671.2:g.136390000A=	GRCh38
NC_000009.11:g.139284452A= , CM000671.1:g.139284452A=	GRCh37
NC_000009.10:g.138404273A=	NCBI36
NG_051233.1:g.15221T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000637388.2:c.976-1409T=	ENSP00000490037.2:n.976-1409T=
ENST00000682698.1:n.861-1409T=
ENST00000684778.1:c.976-1409T= MANE Select	ENSP00000510559.1:n.976-1409T=
ENST00000689006.1:c.*217-1409T=	ENSP00000509362.1:n.*217-1409T=
ENST00000637388.1:c.976-1409T=	ENSP00000490037.1:n.976-1409T=
ENST00000298532.2:c.976-1409T=	ENSP00000298532.2:n.976-1409T=
NM_003086.2:c.976-1409T=	NP_003077.2:n.976-1409T=
XM_005266096.1:c.976-1409T=	XP_005266153.1:n.976-1409T=
XM_006717241.1:c.976-1409T=	XP_006717304.1:n.976-1409T=
XM_006717242.2:c.976-1409T=	XP_006717305.1:n.976-1409T=
XM_006717243.2:c.976-1409T=	XP_006717306.1:n.976-1409T=
XM_011518941.1:c.976-1409T=	XP_011517243.1:n.976-1409T=
XR_428535.1:n.1060-1409T=
NM_003086.3:c.976-1409T=	NP_003077.2:n.976-1409T=
XM_005266096.3:c.976-1409T=	XP_005266153.1:n.976-1409T=
XM_006717241.3:c.976-1409T=	XP_006717304.1:n.976-1409T=
XM_006717242.4:c.976-1409T=	XP_006717305.1:n.976-1409T=
XM_017015058.2:c.976-1409T=	XP_016870547.1:n.976-1409T=
XR_001746368.1:n.2501-1409T=
XR_001746369.1:n.2493-1409T=
NM_001394201.1:c.976-1409T=	NP_001381130.1:n.976-1409T=
NM_001394202.1:c.976-1409T=	NP_001381131.1:n.976-1409T=
NM_001394203.1:c.976-1409T=	NP_001381132.1:n.976-1409T=
NM_003086.4:c.976-1409T= MANE Select	NP_003077.2:n.976-1409T=