Canonical Allele Identifier: CA1723965502
Gene: STEAP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.88297923T= , CM000669.2:g.88297923T= GRCh38
NC_000007.13:g.87927238T= , CM000669.1:g.87927238T= GRCh37
NC_000007.12:g.87765174T= NCBI36
NG_028313.1:g.13991A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380079.9:c.-3+8869A= MANE Select ENSP00000369419.4:n.-3+8869A=
ENST00000301959.9:c.-3+8869A= ENSP00000305545.5:n.-3+8869A=
ENST00000380079.8:c.-3+8869A= ENSP00000369419.4:n.-3+8869A=
ENST00000414498.1:c.-101-6909A= ENSP00000394399.1:n.-101-6909A=
NM_001205315.1:c.-101-6909A= NP_001192244.1:n.-101-6909A=
NM_001205316.1:c.-3+8869A= NP_001192245.1:n.-3+8869A=
NM_024636.3:c.-3+8869A= NP_078912.2:n.-3+8869A=
NM_001205315.2:c.-101-6909A= NP_001192244.1:n.-101-6909A=
NM_001205316.2:c.-3+8869A= NP_001192245.1:n.-3+8869A=
NM_024636.4:c.-3+8869A= MANE Select NP_078912.2:n.-3+8869A=