Canonical Allele Identifier: CA1729348500
Gene: AP4M1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100103553G>T , CM000669.2:g.100103553G>T GRCh38
NC_000007.13:g.99701176G>T , CM000669.1:g.99701176G>T GRCh37
NC_000007.12:g.99539112G>T NCBI36
NG_016312.1:g.7047G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000445295.2:c.462+34G>T ENSP00000393723.2:n.462+34G>T
ENST00000495154.2:n.721+34G>T
ENST00000713591.1:c.462+34G>T ENSP00000518888.1:n.462+34G>T
ENST00000359593.9:c.462+34G>T MANE Select ENSP00000352603.4:n.462+34G>T
ENST00000359593.8:c.462+34G>T ENSP00000352603.4:n.462+34G>T
ENST00000394061.7:c.*415+34G>T ENSP00000377625.3:n.*415+34G>T
ENST00000416938.5:c.418+34G>T
ENST00000421755.5:c.462+34G>T ENSP00000412185.1:n.462+34G>T
ENST00000422582.5:c.78+34G>T ENSP00000406676.1:n.78+34G>T
ENST00000429084.5:c.483+34G>T ENSP00000403663.1:n.483+34G>T
ENST00000438383.5:c.258+34G>T ENSP00000401613.1:n.258+34G>T
ENST00000439416.5:c.330+34G>T ENSP00000414286.1:n.330+34G>T
ENST00000445208.5:c.*71+34G>T ENSP00000400598.1:n.*71+34G>T
ENST00000446007.5:c.462+34G>T ENSP00000396928.1:n.462+34G>T
ENST00000463195.5:n.536+34G>T
NM_004722.3:c.462+34G>T NP_004713.2:n.462+34G>T
XM_005250689.3:c.483+34G>T XP_005250746.1:n.483+34G>T
XM_005250690.3:c.258+34G>T XP_005250747.1:n.258+34G>T
XM_006716175.2:c.483+34G>T XP_006716238.1:n.483+34G>T
XM_011516685.1:c.483+34G>T XP_011514987.1:n.483+34G>T
XM_011516686.1:c.78+34G>T XP_011514988.1:n.78+34G>T
XM_011516687.1:c.-147+34G>T XP_011514989.1:n.-147+34G>T
NM_001363671.1:c.483+34G>T NP_001350600.1:n.483+34G>T
XM_005250689.4:c.483+34G>T XP_005250746.1:n.483+34G>T
XM_005250690.4:c.258+34G>T XP_005250747.1:n.258+34G>T
XM_006716175.4:c.483+34G>T XP_006716238.1:n.483+34G>T
XM_017012790.2:c.78+34G>T XP_016868279.1:n.78+34G>T
XM_017012791.2:c.-147+34G>T XP_016868280.1:n.-147+34G>T
XM_024446995.1:c.462+34G>T XP_024302763.1:n.462+34G>T
XM_024446996.1:c.-147+34G>T XP_024302764.1:n.-147+34G>T
NM_004722.4:c.462+34G>T MANE Select NP_004713.2:n.462+34G>T
NM_001363671.2:c.483+34G>T NP_001350600.1:n.483+34G>T