Canonical Allele Identifier: CA372620027

Gene: SLC39A4

Linked Data

• MyVariant Identifiers: chr8:g.145639434G>A (hg19) ; chr8:g.144414050G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414050G>A , CM000670.2:g.144414050G>A	GRCh38
NC_000008.10:g.145639434G>A , CM000670.1:g.145639434G>A	GRCh37
NC_000008.9:g.145610242G>A	NCBI36
NG_012234.2:g.7841C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1195C>T MANE Select	ENSP00000301305.4:p.Pro399Ser
ENST00000276833.9:c.1120C>T	ENSP00000276833.5:p.Pro374Ser
ENST00000301305.7:c.1195C>T	ENSP00000301305.3:p.Pro399Ser
ENST00000531789.1:n.32C>T
NM_017767.2:c.1120C>T	NP_060237.2:p.Pro374Ser
NM_130849.3:c.1195C>T	NP_570901.2:p.Pro399Ser
XM_006716599.1:c.1195C>T	XP_006716662.1:p.Pro399Ser
XM_011517153.1:c.913C>T	XP_011515455.1:p.Pro305Ser
XM_024447188.1:c.913C>T	XP_024302956.1:p.Pro305Ser
XM_024447189.1:c.913C>T	XP_024302957.1:p.Pro305Ser
NM_001374839.1:c.913C>T	NP_001361768.1:p.Pro305Ser
NM_017767.3:c.1120C>T	NP_060237.3:p.Pro374Ser
NM_130849.4:c.1195C>T MANE Select	NP_570901.3:p.Pro399Ser