Canonical Allele Identifier: CA1723965508
Gene: STEAP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.88297937G= , CM000669.2:g.88297937G= GRCh38
NC_000007.13:g.87927252G= , CM000669.1:g.87927252G= GRCh37
NC_000007.12:g.87765188G= NCBI36
NG_028313.1:g.13977C=

Transcript Alleles

HGVS Amino-acid change
ENST00000380079.9:c.-3+8855C= MANE Select ENSP00000369419.4:n.-3+8855C=
ENST00000301959.9:c.-3+8855C= ENSP00000305545.5:n.-3+8855C=
ENST00000380079.8:c.-3+8855C= ENSP00000369419.4:n.-3+8855C=
ENST00000414498.1:c.-101-6923C= ENSP00000394399.1:n.-101-6923C=
NM_001205315.1:c.-101-6923C= NP_001192244.1:n.-101-6923C=
NM_001205316.1:c.-3+8855C= NP_001192245.1:n.-3+8855C=
NM_024636.3:c.-3+8855C= NP_078912.2:n.-3+8855C=
NM_001205315.2:c.-101-6923C= NP_001192244.1:n.-101-6923C=
NM_001205316.2:c.-3+8855C= NP_001192245.1:n.-3+8855C=
NM_024636.4:c.-3+8855C= MANE Select NP_078912.2:n.-3+8855C=