Canonical Allele Identifier: CA755192667

Gene: MERTK

Linked Data

• dbSNP Id: rs1340847199
• MyVariant Identifiers: chr2:g.112665190_112665191del (hg19) ; chr2:g.111907613_111907614del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111907615_111907616del , CM000664.2:g.111907615_111907616del	GRCh38
NC_000002.11:g.112665192_112665193del , CM000664.1:g.112665192_112665193del	GRCh37
NC_000002.10:g.112381663_112381664del	NCBI36
NG_011607.1:g.14002_14003del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295408.9:c.61+8819_61+8820del MANE Select	ENSP00000295408.4:n.61+8819_61+8820del
ENST00000295408.8:c.61+8819_61+8820del	ENSP00000295408.4:n.61+8819_61+8820del
ENST00000409780.5:c.-47+8819_-47+8820del	ENSP00000387277.1:n.-47+8819_-47+8820del
ENST00000421804.6:c.61+8819_61+8820del	ENSP00000389152.2:n.61+8819_61+8820del
ENST00000439966.5:c.61+8819_61+8820del	ENSP00000402129.1:n.61+8819_61+8820del
ENST00000616902.4:c.-1155+8819_-1155+8820del	ENSP00000482824.1:n.-1155+8819_-1155+8820...
NM_006343.2:c.61+8819_61+8820del	NP_006334.2:n.61+8819_61+8820del
XM_005263565.3:c.61+8819_61+8820del	XP_005263622.1:n.61+8819_61+8820del
XM_005263568.3:c.61+8819_61+8820del	XP_005263625.1:n.61+8819_61+8820del
XM_011510490.1:c.-129+8478_-129+8479del	XP_011508792.1:n.-129+8478_-129+8479del
XM_005263565.4:c.61+8819_61+8820del	XP_005263622.1:n.61+8819_61+8820del
XM_005263568.4:c.61+8819_61+8820del	XP_005263625.1:n.61+8819_61+8820del
XM_011510490.3:c.-129+8478_-129+8479del	XP_011508792.1:n.-129+8478_-129+8479del
XM_017003165.2:c.-1207+8819_-1207+8820del	XP_016858654.1:n.-1207+8819_-1207+8820del...
NM_006343.3:c.61+8819_61+8820del MANE Select	NP_006334.2:n.61+8819_61+8820del