Canonical Allele Identifier: CA372621229

Gene: SLC39A4

Linked Data

• MyVariant Identifiers: chr8:g.145639723G>C (hg19) ; chr8:g.144414339G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414339G>C , CM000670.2:g.144414339G>C	GRCh38
NC_000008.10:g.145639723G>C , CM000670.1:g.145639723G>C	GRCh37
NC_000008.9:g.145610531G>C	NCBI36
NG_012234.2:g.7552C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1072C>G MANE Select	ENSP00000301305.4:p.His358Asp
ENST00000276833.9:c.997C>G	ENSP00000276833.5:p.His333Asp
ENST00000301305.7:c.1072C>G	ENSP00000301305.3:p.His358Asp
NM_017767.2:c.997C>G	NP_060237.2:p.His333Asp
NM_130849.3:c.1072C>G	NP_570901.2:p.His358Asp
XM_006716599.1:c.1072C>G	XP_006716662.1:p.His358Asp
XM_011517153.1:c.790C>G	XP_011515455.1:p.His264Asp
XM_024447188.1:c.790C>G	XP_024302956.1:p.His264Asp
XM_024447189.1:c.790C>G	XP_024302957.1:p.His264Asp
NM_001374839.1:c.790C>G	NP_001361768.1:p.His264Asp
NM_017767.3:c.997C>G	NP_060237.3:p.His333Asp
NM_130849.4:c.1072C>G MANE Select	NP_570901.3:p.His358Asp