Canonical Allele Identifier: CA576138234
Gene: STEAP4 HGNC NCBI

Linked Data

dbSNP Id: rs949863597
gnomAD v2: 7-87927400-G-T
gnomAD v3: 7-88298085-G-T
gnomAD v4: 7-88298085-G-T
MyVariant Identifiers: chr7:g.87927400G>T (hg19) chr7:g.88298085G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.88298085G>T , CM000669.2:g.88298085G>T GRCh38
NC_000007.13:g.87927400G>T , CM000669.1:g.87927400G>T GRCh37
NC_000007.12:g.87765336G>T NCBI36
NG_028313.1:g.13829C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000380079.9:c.-3+8707C>A MANE Select ENSP00000369419.4:n.-3+8707C>A
ENST00000301959.9:c.-3+8707C>A ENSP00000305545.5:n.-3+8707C>A
ENST00000380079.8:c.-3+8707C>A ENSP00000369419.4:n.-3+8707C>A
ENST00000414498.1:c.-101-7071C>A ENSP00000394399.1:n.-101-7071C>A
NM_001205315.1:c.-101-7071C>A NP_001192244.1:n.-101-7071C>A
NM_001205316.1:c.-3+8707C>A NP_001192245.1:n.-3+8707C>A
NM_024636.3:c.-3+8707C>A NP_078912.2:n.-3+8707C>A
NM_001205315.2:c.-101-7071C>A NP_001192244.1:n.-101-7071C>A
NM_001205316.2:c.-3+8707C>A NP_001192245.1:n.-3+8707C>A
NM_024636.4:c.-3+8707C>A MANE Select NP_078912.2:n.-3+8707C>A
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