Canonical Allele Identifier: CA2838196415

Gene: SPAG17

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.118160943A>G , CM000663.2:g.118160943A>G	GRCh38
NC_000001.10:g.118703566A>G , CM000663.1:g.118703566A>G	GRCh37
NC_000001.9:g.118505089A>G	NCBI36
NG_053041.1:g.29283T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336338.10:c.88-9574T>C MANE Select	ENSP00000337804.5:n.88-9574T>C
ENST00000336338.9:c.88-9574T>C	ENSP00000337804.5:n.88-9574T>C
ENST00000465053.1:n.154-9574T>C
NM_206996.2:c.88-9574T>C	NP_996879.1:n.88-9574T>C
XM_006710426.2:c.88-9574T>C	XP_006710489.1:n.88-9574T>C
XM_006710427.2:c.88-9574T>C	XP_006710490.1:n.88-9574T>C
XM_011540934.1:c.88-9574T>C	XP_011539236.1:n.88-9574T>C
XM_011540938.1:c.88-9574T>C	XP_011539240.1:n.88-9574T>C
XR_946574.1:n.156-9574T>C
NM_206996.3:c.88-9574T>C	NP_996879.1:n.88-9574T>C
XM_006710426.3:c.88-9574T>C	XP_006710489.1:n.88-9574T>C
XM_006710427.3:c.88-9574T>C	XP_006710490.1:n.88-9574T>C
NM_206996.4:c.88-9574T>C MANE Select	NP_996879.1:n.88-9574T>C