Canonical Allele Identifier: CA309941890

Gene: ZNF600

Linked Data

• dbSNP Id: rs145170652
• gnomAD v2: 19-53283985-AAAAC-A
• gnomAD v3: 19-52780732-AAAAC-A
• gnomAD v4: 19-52780732-AAAAC-A
• MyVariant Identifiers: chr19:g.53283990_53283993del (hg19) ; chr19:g.53283986_53283989del (hg19) ; chr19:g.52780737_52780740del (hg38) ; chr19:g.52780733_52780736del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52780748_52780751del , CM000681.2:g.52780748_52780751del	GRCh38
NC_000019.9:g.53284001_53284004del , CM000681.1:g.53284001_53284004del	GRCh37
NC_000019.8:g.57975813_57975816del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000685388.1:c.-19-1829_-19-1826del	ENSP00000510246.1:n.-19-1829_-19-1826del
ENST00000688329.1:c.-162-13_-162-10del	ENSP00000509375.1:n.-162-13_-162-10del
ENST00000692063.1:c.-175_-172del MANE Select	ENSP00000509267.1:n.-175_-172del
ENST00000647907.1:c.-19-1829_-19-1826del	ENSP00000497989.1:n.-19-1829_-19-1826del
ENST00000648893.1:c.-20+581_-20+584del	ENSP00000497895.1:n.-20+581_-20+584del
ENST00000648973.1:c.-19-1829_-19-1826del	ENSP00000497540.1:n.-19-1829_-19-1826del
ENST00000338230.3:c.-99-1829_-99-1826del	ENSP00000344791.2:n.-99-1829_-99-1826del
ENST00000360272.5:c.824-13723_824-13720del	ENSP00000353410.5:n.824-13723_824-13720del
ENST00000599893.1:n.517_520del
NM_198457.2:c.-99-1829_-99-1826del	NP_940859.2:n.-99-1829_-99-1826del
XM_005258576.3:c.-19-1829_-19-1826del	XP_005258633.1:n.-19-1829_-19-1826del
XM_006723055.2:c.-19-1829_-19-1826del	XP_006723118.1:n.-19-1829_-19-1826del
XM_006723057.2:c.64-6035_64-6032del	XP_006723120.1:n.64-6035_64-6032del
XM_006723058.2:c.64-6035_64-6032del	XP_006723121.1:n.64-6035_64-6032del
XM_011526563.1:c.-175_-172del	XP_011524865.1:n.-175_-172del
XM_011526564.1:c.-20+581_-20+584del	XP_011524866.1:n.-20+581_-20+584del
XM_011526565.1:c.-20+581_-20+584del	XP_011524867.1:n.-20+581_-20+584del
XM_011526566.1:c.-255_-252del	XP_011524868.1:n.-255_-252del
NM_001321866.1:c.-175_-172del	NP_001308795.1:n.-175_-172del
NM_001321867.1:c.-19-1829_-19-1826del	NP_001308796.1:n.-19-1829_-19-1826del
NM_198457.3:c.-99-1829_-99-1826del	NP_940859.3:n.-99-1829_-99-1826del
XM_017026390.1:c.-162-13_-162-10del	XP_016881879.1:n.-162-13_-162-10del
XM_017026391.1:c.-175_-172del	XP_016881880.1:n.-175_-172del
XM_017026392.1:c.-162-13_-162-10del	XP_016881881.1:n.-162-13_-162-10del
NM_001321866.2:c.-175_-172del	NP_001308795.1:n.-175_-172del
NM_001321867.2:c.-19-1829_-19-1826del	NP_001308796.1:n.-19-1829_-19-1826del
NM_198457.4:c.-99-1829_-99-1826del	NP_940859.3:n.-99-1829_-99-1826del
NM_001321866.3:c.-175_-172del	NP_001308795.1:n.-175_-172del
NM_001321867.3:c.-19-1829_-19-1826del	NP_001308796.1:n.-19-1829_-19-1826del
NM_198457.5:c.-99-1829_-99-1826del	NP_940859.3:n.-99-1829_-99-1826del
NM_001321866.4:c.-175_-172del MANE Select	NP_001308795.1:n.-175_-172del