Canonical Allele Identifier: CA2627716045
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38349564_38349565insTTA , CM000677.2:g.38349564_38349565insTTA GRCh38
NC_000015.9:g.38641765_38641766insTTA , CM000677.1:g.38641765_38641766insTTA GRCh37
NC_000015.8:g.36429057_36429058insTTA NCBI36
NG_008980.1:g.101714_101715insTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.684+41_684+42insTTA MANE Select ENSP00000299084.4:n.684+41_684+42insTTA
ENST00000299084.8:c.684+41_684+42insTTA ENSP00000299084.4:n.684+41_684+42insTTA
NM_152594.2:c.684+41_684+42insTTA NP_689807.1:n.684+41_684+42insTTA
XM_005254202.2:c.720+41_720+42insTTA XP_005254259.1:n.720+41_720+42insTTA
XM_005254203.3:c.462+41_462+42insTTA XP_005254260.1:n.462+41_462+42insTTA
XM_011521288.1:c.621+41_621+42insTTA XP_011519590.1:n.621+41_621+42insTTA
XM_011521289.1:c.621+41_621+42insTTA XP_011519591.1:n.621+41_621+42insTTA
XM_011521290.1:c.621+41_621+42insTTA XP_011519592.1:n.621+41_621+42insTTA
XM_005254202.3:c.720+41_720+42insTTA XP_005254259.1:n.720+41_720+42insTTA
XM_011521289.3:c.621+41_621+42insTTA XP_011519591.1:n.621+41_621+42insTTA
NM_152594.3:c.684+41_684+42insTTA MANE Select NP_689807.1:n.684+41_684+42insTTA