Canonical Allele Identifier: CA1279526476
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111907668_111907669delinsAG , CM000664.2:g.111907668_111907669delinsAG GRCh38
NC_000002.11:g.112665245_112665246delinsAG , CM000664.1:g.112665245_112665246delinsAG GRCh37
NC_000002.10:g.112381716_112381717delinsAG NCBI36
NG_011607.1:g.14055_14056delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000295408.9:c.61+8872_61+8873delinsAG MANE Select ENSP00000295408.4:n.61+8872_61+8873delins...
ENST00000295408.8:c.61+8872_61+8873delinsAG ENSP00000295408.4:n.61+8872_61+8873delins...
ENST00000409780.5:c.-47+8872_-47+8873delinsAG ENSP00000387277.1:n.-47+8872_-47+8873deli...
ENST00000421804.6:c.61+8872_61+8873delinsAG ENSP00000389152.2:n.61+8872_61+8873delins...
ENST00000439966.5:c.61+8872_61+8873delinsAG ENSP00000402129.1:n.61+8872_61+8873delins...
ENST00000616902.4:c.-1155+8872_-1155+8873delinsAG ENSP00000482824.1:n.-1155+8872_-1155+8873...
NM_006343.2:c.61+8872_61+8873delinsAG NP_006334.2:n.61+8872_61+8873delinsAG
XM_005263565.3:c.61+8872_61+8873delinsAG XP_005263622.1:n.61+8872_61+8873delinsAG
XM_005263568.3:c.61+8872_61+8873delinsAG XP_005263625.1:n.61+8872_61+8873delinsAG
XM_011510490.1:c.-129+8531_-129+8532delinsAG XP_011508792.1:n.-129+8531_-129+8532delin...
XM_005263565.4:c.61+8872_61+8873delinsAG XP_005263622.1:n.61+8872_61+8873delinsAG
XM_005263568.4:c.61+8872_61+8873delinsAG XP_005263625.1:n.61+8872_61+8873delinsAG
XM_011510490.3:c.-129+8531_-129+8532delinsAG XP_011508792.1:n.-129+8531_-129+8532delin...
XM_017003165.2:c.-1207+8872_-1207+8873delinsAG XP_016858654.1:n.-1207+8872_-1207+8873del...
NM_006343.3:c.61+8872_61+8873delinsAG MANE Select NP_006334.2:n.61+8872_61+8873delinsAG