Canonical Allele Identifier: CA1723965505
Gene: STEAP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.88297931C= , CM000669.2:g.88297931C= GRCh38
NC_000007.13:g.87927246C= , CM000669.1:g.87927246C= GRCh37
NC_000007.12:g.87765182C= NCBI36
NG_028313.1:g.13983G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380079.9:c.-3+8861G= MANE Select ENSP00000369419.4:n.-3+8861G=
ENST00000301959.9:c.-3+8861G= ENSP00000305545.5:n.-3+8861G=
ENST00000380079.8:c.-3+8861G= ENSP00000369419.4:n.-3+8861G=
ENST00000414498.1:c.-101-6917G= ENSP00000394399.1:n.-101-6917G=
NM_001205315.1:c.-101-6917G= NP_001192244.1:n.-101-6917G=
NM_001205316.1:c.-3+8861G= NP_001192245.1:n.-3+8861G=
NM_024636.3:c.-3+8861G= NP_078912.2:n.-3+8861G=
NM_001205315.2:c.-101-6917G= NP_001192244.1:n.-101-6917G=
NM_001205316.2:c.-3+8861G= NP_001192245.1:n.-3+8861G=
NM_024636.4:c.-3+8861G= MANE Select NP_078912.2:n.-3+8861G=