Canonical Allele Identifier: CA1969373837

Gene: SLC39A13

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47415283C= , CM000673.2:g.47415283C=	GRCh38
NC_000011.9:g.47436834C= , CM000673.1:g.47436834C=	GRCh37
NC_000011.8:g.47393410C=	NCBI36
NG_017073.1:g.11789C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362021.9:c.1041-5C= MANE Select	ENSP00000354689.4:n.1041-5C=
ENST00000354884.8:c.1020-5C=	ENSP00000346956.4:n.1020-5C=
ENST00000362021.8:c.1041-5C=	ENSP00000354689.4:n.1041-5C=
ENST00000524886.1:n.299-5C=
ENST00000524928.1:c.*1366C=	ENSP00000437186.1:n.*1366C=
ENST00000527829.1:n.396C=
ENST00000533076.5:c.*38-5C=	ENSP00000434290.1:n.*38-5C=
NM_001128225.2:c.1041-5C=	NP_001121697.1:n.1041-5C=
NM_152264.4:c.1020-5C=	NP_689477.2:n.1020-5C=
XM_006718381.2:c.1065-5C=	XP_006718444.1:n.1065-5C=
XM_006718383.2:c.957-5C=	XP_006718446.1:n.957-5C=
XM_006718384.2:c.*38-5C=	XP_006718447.1:n.*38-5C=
XM_006718385.2:c.*38-5C=	XP_006718448.1:n.*38-5C=
XM_011520466.1:c.1086-5C=	XP_011518768.1:n.1086-5C=
XM_011520467.1:c.1041-5C=	XP_011518769.1:n.1041-5C=
XM_011520468.1:c.1041-5C=	XP_011518770.1:n.1041-5C=
XM_011520469.1:c.978-5C=	XP_011518771.1:n.978-5C=
XM_011520470.1:c.933-5C=	XP_011518772.1:n.933-5C=
XR_242832.1:n.1426-5C=
XR_428862.2:n.1101-5C=
XR_428863.2:n.1097-5C=
XR_930928.1:n.1122-5C=
NM_001330245.1:c.*38-5C=	NP_001317174.1:n.*38-5C=
NR_134854.1:n.1282-5C=
XM_006718381.3:c.1065-5C=	XP_006718444.1:n.1065-5C=
XM_006718383.3:c.957-5C=	XP_006718446.1:n.957-5C=
XM_011520468.3:c.1041-5C=	XP_011518770.1:n.1041-5C=
XM_011520470.2:c.933-5C=	XP_011518772.1:n.933-5C=
XM_017018540.2:c.1020-5C=	XP_016874029.1:n.1020-5C=
XM_017018541.2:c.912-5C=	XP_016874030.1:n.912-5C=
XM_024448762.1:c.1170-5C=	XP_024304530.1:n.1170-5C=
XR_001748027.1:n.1241-5C=
XR_001748028.1:n.1223-5C=
XR_428862.3:n.1101-5C=
XR_428863.3:n.1097-5C=
XR_930928.2:n.1122-5C=
NM_001128225.3:c.1041-5C= MANE Select	NP_001121697.2:n.1041-5C=
NM_001330245.2:c.*38-5C=	NP_001317174.2:n.*38-5C=
NM_152264.5:c.1020-5C=	NP_689477.3:n.1020-5C=