Canonical Allele Identifier: CA15792566

Gene: SLC46A3

Genomic Alleles

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

Transcript Alleles

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