Canonical Allele Identifier: CA2553443165
Gene: STEAP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.88297925_88297926insC , CM000669.2:g.88297925_88297926insC GRCh38
NC_000007.13:g.87927240_87927241insC , CM000669.1:g.87927240_87927241insC GRCh37
NC_000007.12:g.87765176_87765177insC NCBI36
NG_028313.1:g.13988_13989insG

Transcript Alleles

HGVS Amino-acid change
ENST00000380079.9:c.-3+8866_-3+8867insG MANE Select ENSP00000369419.4:n.-3+8866_-3+8867insG
ENST00000301959.9:c.-3+8866_-3+8867insG ENSP00000305545.5:n.-3+8866_-3+8867insG
ENST00000380079.8:c.-3+8866_-3+8867insG ENSP00000369419.4:n.-3+8866_-3+8867insG
ENST00000414498.1:c.-101-6912_-101-6911insG ENSP00000394399.1:n.-101-6912_-101-6911insG
NM_001205315.1:c.-101-6912_-101-6911insG NP_001192244.1:n.-101-6912_-101-6911insG
NM_001205316.1:c.-3+8866_-3+8867insG NP_001192245.1:n.-3+8866_-3+8867insG
NM_024636.3:c.-3+8866_-3+8867insG NP_078912.2:n.-3+8866_-3+8867insG
NM_001205315.2:c.-101-6912_-101-6911insG NP_001192244.1:n.-101-6912_-101-6911insG
NM_001205316.2:c.-3+8866_-3+8867insG NP_001192245.1:n.-3+8866_-3+8867insG
NM_024636.4:c.-3+8866_-3+8867insG MANE Select NP_078912.2:n.-3+8866_-3+8867insG