Canonical Allele Identifier: CA2751719925
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112008551_112008552insACA , CM000664.2:g.112008551_112008552insACA GRCh38
NC_000002.11:g.112766128_112766129insACA , CM000664.1:g.112766128_112766129insACA GRCh37
NC_000002.10:g.112482599_112482600insACA NCBI36
NG_011607.1:g.114938_114939insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.1960+76_1960+77insACA MANE Select ENSP00000295408.4:n.1960+76_1960+77insACA
ENST00000295408.8:c.1960+76_1960+77insACA ENSP00000295408.4:n.1960+76_1960+77insACA
ENST00000409780.5:c.1432+76_1432+77insACA ENSP00000387277.1:n.1432+76_1432+77insACA
ENST00000421804.6:c.1960+76_1960+77insACA ENSP00000389152.2:n.1960+76_1960+77insACA
ENST00000439966.5:c.*1433+76_*1433+77insACA ENSP00000402129.1:n.*1433+76_*1433+77insACA
ENST00000616902.4:c.925+76_925+77insACA ENSP00000482824.1:n.925+76_925+77insACA
NM_006343.2:c.1960+76_1960+77insACA NP_006334.2:n.1960+76_1960+77insACA
XM_005263565.3:c.1960+76_1960+77insACA XP_005263622.1:n.1960+76_1960+77insACA
XM_005263568.3:c.1960+76_1960+77insACA XP_005263625.1:n.1960+76_1960+77insACA
XM_011510490.1:c.1771+76_1771+77insACA XP_011508792.1:n.1771+76_1771+77insACA
XM_011510491.1:c.745+76_745+77insACA XP_011508793.1:n.745+76_745+77insACA
XM_005263565.4:c.1960+76_1960+77insACA XP_005263622.1:n.1960+76_1960+77insACA
XM_005263568.4:c.1960+76_1960+77insACA XP_005263625.1:n.1960+76_1960+77insACA
XM_011510490.3:c.1771+76_1771+77insACA XP_011508792.1:n.1771+76_1771+77insACA
XM_017003164.1:c.1771+76_1771+77insACA XP_016858653.1:n.1771+76_1771+77insACA
XM_017003165.2:c.745+76_745+77insACA XP_016858654.1:n.745+76_745+77insACA
NM_006343.3:c.1960+76_1960+77insACA MANE Select NP_006334.2:n.1960+76_1960+77insACA