Canonical Allele Identifier: CA1336472024
Gene: SH3BP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.234991569A= , CM000664.2:g.234991569A= GRCh38
NC_000002.11:g.235900213A= , CM000664.1:g.235900213A= GRCh37
NC_000002.10:g.235564952A= NCBI36
NG_033930.1:g.44586A=

Transcript Alleles

HGVS Amino-acid change
ENST00000392011.7:c.-206-3734A= MANE Select ENSP00000375867.2:n.-206-3734A=
ENST00000344528.8:c.-122-3734A= ENSP00000340237.4:n.-122-3734A=
ENST00000392011.6:c.-206-3734A= ENSP00000375867.2:n.-206-3734A=
ENST00000409212.5:c.-206-3734A= ENSP00000386862.1:n.-206-3734A=
ENST00000416021.5:c.-133+39399A= ENSP00000403251.1:n.-133+39399A=
ENST00000444916.5:c.-206-3734A= ENSP00000387995.1:n.-206-3734A=
ENST00000446904.5:c.-206-3734A= ENSP00000415391.1:n.-206-3734A=
ENST00000462602.6:n.149-3734A=
NM_014521.2:c.-206-3734A= NP_055336.1:n.-206-3734A=
XM_011510891.1:c.-206-3734A= XP_011509193.1:n.-206-3734A=
XM_011510892.1:c.-206-3734A= XP_011509194.1:n.-206-3734A=
XM_011510894.1:c.-206-3734A= XP_011509196.1:n.-206-3734A=
XM_011510891.2:c.-206-3734A= XP_011509193.1:n.-206-3734A=
XM_011510894.2:c.-206-3734A= XP_011509196.1:n.-206-3734A=
NM_014521.3:c.-206-3734A= MANE Select NP_055336.1:n.-206-3734A=
NM_001371302.1:c.-206-3734A= NP_001358231.1:n.-206-3734A=
NM_001371303.1:c.-206-3734A= NP_001358232.1:n.-206-3734A=
NM_001371304.1:c.-122-3734A= NP_001358233.1:n.-122-3734A=
NM_001371305.1:c.-206-3734A= NP_001358234.1:n.-206-3734A=