Canonical Allele Identifier: CA197429304

Gene: FSD1L

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.105539204T>C , CM000671.2:g.105539204T>C	GRCh38
NC_000009.11:g.108301485T>C , CM000671.1:g.108301485T>C	GRCh37
NC_000009.10:g.107341306T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001145313.3:c.1379-59T>C MANE Select	NP_001138785.1:n.1379-59T>C
ENST00000481272.6:c.1379-59T>C MANE Select	ENSP00000417492.1:n.1379-59T>C
NM_001145313.2:c.1379-59T>C	NP_001138785.1:n.1379-59T>C
NM_001287191.1:c.1313-59T>C	NP_001274120.1:n.1313-59T>C
NM_001287191.2:c.1313-59T>C	NP_001274120.1:n.1313-59T>C
NM_001287192.1:c.1280-59T>C	NP_001274121.1:n.1280-59T>C
NM_001287192.2:c.1280-59T>C	NP_001274121.1:n.1280-59T>C
NM_001330739.1:c.1316-59T>C	NP_001317668.1:n.1316-59T>C
NM_001330739.2:c.1316-59T>C	NP_001317668.1:n.1316-59T>C
ENST00000374707.1:c.722-59T>C	ENSP00000363839.1:n.722-59T>C
ENST00000374710.7:c.1313-59T>C	ENSP00000363842.4:n.1313-59T>C
ENST00000394926.7:c.1316-59T>C	ENSP00000378384.3:n.1316-59T>C
ENST00000481272.5:c.1379-59T>C	ENSP00000417492.1:n.1379-59T>C
ENST00000484973.5:c.1280-59T>C	ENSP00000419691.1:n.1280-59T>C
XM_005252254.2:c.1412-59T>C	XP_005252311.1:n.1412-59T>C
XM_005252257.3:c.1316-59T>C	XP_005252314.1:n.1316-59T>C
XM_005252260.3:c.941-59T>C	XP_005252317.1:n.941-59T>C
XM_011519077.1:c.1430-59T>C	XP_011517379.1:n.1430-59T>C
XM_011519077.2:c.1430-59T>C	XP_011517379.1:n.1430-59T>C
XM_011519078.1:c.1409-59T>C	XP_011517380.1:n.1409-59T>C
XM_011519078.2:c.1418-59T>C	XP_011517380.2:n.1418-59T>C
XM_011519079.1:c.1406-59T>C	XP_011517381.1:n.1406-59T>C
XM_011519079.2:c.1415-59T>C	XP_011517381.2:n.1415-59T>C
XM_011519080.1:c.755-59T>C	XP_011517382.1:n.755-59T>C
XM_011519080.2:c.755-59T>C	XP_011517382.1:n.755-59T>C
XM_011519081.1:c.722-59T>C	XP_011517383.1:n.722-59T>C
XM_011519081.2:c.722-59T>C	XP_011517383.1:n.722-59T>C
XM_017015182.1:c.1376-59T>C	XP_016870671.1:n.1376-59T>C
XM_017015183.1:c.1283-59T>C	XP_016870672.1:n.1283-59T>C
XM_017015184.1:c.941-59T>C	XP_016870673.1:n.941-59T>C
XM_017015185.1:c.1065-7154T>C	XP_016870674.1:n.1065-7154T>C
XM_017015187.1:c.930-7154T>C	XP_016870676.1:n.930-7154T>C
XM_024447690.1:c.908-59T>C	XP_024303458.1:n.908-59T>C