Canonical Allele Identifier: CA1279526462

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111907643G= , CM000664.2:g.111907643G=	GRCh38
NC_000002.11:g.112665220G= , CM000664.1:g.112665220G=	GRCh37
NC_000002.10:g.112381691G=	NCBI36
NG_011607.1:g.14030G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295408.9:c.61+8847G= MANE Select	ENSP00000295408.4:n.61+8847G=
ENST00000295408.8:c.61+8847G=	ENSP00000295408.4:n.61+8847G=
ENST00000409780.5:c.-47+8847G=	ENSP00000387277.1:n.-47+8847G=
ENST00000421804.6:c.61+8847G=	ENSP00000389152.2:n.61+8847G=
ENST00000439966.5:c.61+8847G=	ENSP00000402129.1:n.61+8847G=
ENST00000616902.4:c.-1155+8847G=	ENSP00000482824.1:n.-1155+8847G=
NM_006343.2:c.61+8847G=	NP_006334.2:n.61+8847G=
XM_005263565.3:c.61+8847G=	XP_005263622.1:n.61+8847G=
XM_005263568.3:c.61+8847G=	XP_005263625.1:n.61+8847G=
XM_011510490.1:c.-129+8506G=	XP_011508792.1:n.-129+8506G=
XM_005263565.4:c.61+8847G=	XP_005263622.1:n.61+8847G=
XM_005263568.4:c.61+8847G=	XP_005263625.1:n.61+8847G=
XM_011510490.3:c.-129+8506G=	XP_011508792.1:n.-129+8506G=
XM_017003165.2:c.-1207+8847G=	XP_016858654.1:n.-1207+8847G=
NM_006343.3:c.61+8847G= MANE Select	NP_006334.2:n.61+8847G=