Canonical Allele Identifier: CA2018024275

Gene: SLC46A3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28704313T>G , CM000675.2:g.28704313T>G	GRCh38
NC_000013.10:g.29278450T>G , CM000675.1:g.29278450T>G	GRCh37
NC_000013.9:g.28176450T>G	NCBI36
NG_053189.1:g.19701A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266943.11:c.1145-214A>C MANE Select	ENSP00000266943.7:n.1145-214A>C
ENST00000266943.10:c.1145-214A>C	ENSP00000266943.6:n.1145-214A>C
ENST00000380814.4:c.1145-214A>C	ENSP00000370192.4:n.1145-214A>C
ENST00000475385.1:n.245A>C
NM_001135919.1:c.1145-214A>C	NP_001129391.1:n.1145-214A>C
NM_181785.3:c.1145-214A>C	NP_861450.1:n.1145-214A>C
XM_005266361.1:c.1145-214A>C	XP_005266418.1:n.1145-214A>C
NM_001347960.1:c.1145-214A>C	NP_001334889.1:n.1145-214A>C
XM_005266361.2:c.1145-214A>C	XP_005266418.1:n.1145-214A>C
NM_001135919.2:c.1145-214A>C	NP_001129391.1:n.1145-214A>C
NM_181785.4:c.1145-214A>C MANE Select	NP_861450.1:n.1145-214A>C
NM_001347960.2:c.1145-214A>C	NP_001334889.1:n.1145-214A>C