Canonical Allele Identifier: CA1120276484

Gene: SLC39A4

Linked Data

• dbSNP Id: rs1822055212
• gnomAD v3: 8-144414176-G-A
• gnomAD v4: 8-144414176-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144414176G>A , CM000670.2:g.144414176G>A	GRCh38
NC_000008.10:g.145639560G>A , CM000670.1:g.145639560G>A	GRCh37
NC_000008.9:g.145610368G>A	NCBI36
NG_012234.2:g.7715C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301305.8:c.1150-81C>T MANE Select	ENSP00000301305.4:n.1150-81C>T
ENST00000276833.9:c.1075-81C>T	ENSP00000276833.5:n.1075-81C>T
ENST00000301305.7:c.1150-81C>T	ENSP00000301305.3:n.1150-81C>T
NM_017767.2:c.1075-81C>T	NP_060237.2:n.1075-81C>T
NM_130849.3:c.1150-81C>T	NP_570901.2:n.1150-81C>T
XM_006716599.1:c.1150-81C>T	XP_006716662.1:n.1150-81C>T
XM_011517153.1:c.868-81C>T	XP_011515455.1:n.868-81C>T
XM_024447188.1:c.868-81C>T	XP_024302956.1:n.868-81C>T
XM_024447189.1:c.868-81C>T	XP_024302957.1:n.868-81C>T
NM_001374839.1:c.868-81C>T	NP_001361768.1:n.868-81C>T
NM_017767.3:c.1075-81C>T	NP_060237.3:n.1075-81C>T
NM_130849.4:c.1150-81C>T MANE Select	NP_570901.3:n.1150-81C>T