Canonical Allele Identifier: CA725748663

Gene: SPATA33

Linked Data

• dbSNP Id: rs154663
• MyVariant Identifiers: chr16:g.89726035T>G (hg19) ; chr16:g.89659627T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89659627T>G , CM000678.2:g.89659627T>G	GRCh38
NC_000016.9:g.89726035T>G , CM000678.1:g.89726035T>G	GRCh37
NC_000016.8:g.88253536T>G	NCBI36
NG_033005.1:g.3159A>C
NG_033005.2:g.3159A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000579310.6:c.211+1206T>G MANE Select	ENSP00000462996.1:n.211+1206T>G
ENST00000457689.3:c.285+1206T>G	ENSP00000462403.2:n.285+1206T>G
ENST00000564238.2:c.1458T>G	ENSP00000462233.2:n.1458T>G
ENST00000566204.2:c.118+1206T>G	ENSP00000461933.2:n.118+1206T>G
ENST00000301031.8:c.208+1206T>G	ENSP00000301031.4:n.208+1206T>G
ENST00000457689.2:c.285+1206T>G
ENST00000564238.1:c.1458T>G
ENST00000565890.1:c.381+1418T>G	ENSP00000455761.1:n.381+1418T>G
ENST00000566204.1:c.229+1206T>G	ENSP00000461933.1:n.229+1206T>G
ENST00000567827.1:c.418+1050T>G
ENST00000568929.1:c.119-913T>G	ENSP00000462319.1:n.119-913T>G
ENST00000579310.5:c.211+1206T>G	ENSP00000462996.1:n.211+1206T>G
ENST00000611218.1:c.118+1206T>G	ENSP00000481797.1:n.118+1206T>G
NM_001271907.1:c.211+1206T>G	NP_001258836.1:n.211+1206T>G
NM_001271908.1:c.118+1206T>G	NP_001258837.1:n.118+1206T>G
NM_001271909.1:c.118+1206T>G	NP_001258838.1:n.118+1206T>G
NM_001271910.1:c.211+1206T>G	NP_001258839.1:n.211+1206T>G
NM_153025.2:c.208+1206T>G	NP_694570.1:n.208+1206T>G
NR_073515.1:n.406+1418T>G
NR_073516.1:n.376-913T>G
XM_006721133.2:c.212-913T>G	XP_006721196.1:n.212-913T>G
NR_073515.2:n.142+1418T>G
NR_073516.2:n.355-913T>G
NM_001271907.2:c.211+1206T>G MANE Select	NP_001258836.1:n.211+1206T>G
NM_001271908.2:c.118+1206T>G	NP_001258837.1:n.118+1206T>G
NM_001271909.3:c.118+1206T>G	NP_001258838.1:n.118+1206T>G
NM_001271910.2:c.211+1206T>G	NP_001258839.1:n.211+1206T>G
NM_001387226.1:c.241+1176T>G	NP_001374155.1:n.241+1176T>G
NM_153025.3:c.208+1206T>G	NP_694570.1:n.208+1206T>G
NR_073515.3:n.142+1418T>G