Canonical Allele Identifier: CA348229082

Gene: MERTK

Linked Data

• MyVariant Identifiers: chr2:g.112705030A>G (hg19) ; chr2:g.111947453A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947453A>G , CM000664.2:g.111947453A>G	GRCh38
NC_000002.11:g.112705030A>G , CM000664.1:g.112705030A>G	GRCh37
NC_000002.10:g.112421501A>G	NCBI36
NG_011607.1:g.53840A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.643A>G MANE Select	ENSP00000295408.4:p.Asn215Asp
ENST00000295408.8:c.643A>G	ENSP00000295408.4:p.Asn215Asp
ENST00000409780.5:c.115A>G	ENSP00000387277.1:p.Asn39Asp
ENST00000421804.6:c.643A>G	ENSP00000389152.2:p.Asn215Asp
ENST00000439966.5:c.*116A>G	ENSP00000402129.1:n.*116A>G
ENST00000616902.4:c.-573A>G	ENSP00000482824.1:n.-573A>G
NM_006343.2:c.643A>G	NP_006334.2:p.Asn215Asp
XM_005263565.3:c.643A>G	XP_005263622.1:p.Asn215Asp
XM_005263568.3:c.643A>G	XP_005263625.1:p.Asn215Asp
XM_011510490.1:c.454A>G	XP_011508792.1:p.Asn152Asp
XM_005263565.4:c.643A>G	XP_005263622.1:p.Asn215Asp
XM_005263568.4:c.643A>G	XP_005263625.1:p.Asn215Asp
XM_011510490.3:c.454A>G	XP_011508792.1:p.Asn152Asp
XM_017003164.1:c.454A>G	XP_016858653.1:p.Asn152Asp
XM_017003165.2:c.-625A>G	XP_016858654.1:n.-625A>G
NM_006343.3:c.643A>G MANE Select	NP_006334.2:p.Asn215Asp