Canonical Allele Identifier: CA843477430

Gene: STEAP4

Linked Data

• dbSNP Id: rs10263111
• MyVariant Identifiers: chr7:g.87927392G>A (hg19) ; chr7:g.88298077G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.88298077G>A , CM000669.2:g.88298077G>A	GRCh38
NC_000007.13:g.87927392G>A , CM000669.1:g.87927392G>A	GRCh37
NC_000007.12:g.87765328G>A	NCBI36
NG_028313.1:g.13837C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000380079.9:c.-3+8715C>T MANE Select	ENSP00000369419.4:n.-3+8715C>T
ENST00000301959.9:c.-3+8715C>T	ENSP00000305545.5:n.-3+8715C>T
ENST00000380079.8:c.-3+8715C>T	ENSP00000369419.4:n.-3+8715C>T
ENST00000414498.1:c.-101-7063C>T	ENSP00000394399.1:n.-101-7063C>T
NM_001205315.1:c.-101-7063C>T	NP_001192244.1:n.-101-7063C>T
NM_001205316.1:c.-3+8715C>T	NP_001192245.1:n.-3+8715C>T
NM_024636.3:c.-3+8715C>T	NP_078912.2:n.-3+8715C>T
NM_001205315.2:c.-101-7063C>T	NP_001192244.1:n.-101-7063C>T
NM_001205316.2:c.-3+8715C>T	NP_001192245.1:n.-3+8715C>T
NM_024636.4:c.-3+8715C>T MANE Select	NP_078912.2:n.-3+8715C>T